2 Clinical Protocols Jobs nearby Erode

A Medical Director is a senior-level physician who provides clinical leadership and oversight for a healthcare organization. They bridge the gap between clinical operations and business administration, ensuring high-quality patient care, regulatory compliance, and effective resource management. While the specific duties depend on the setting, such as a hospital, clinic, or pharmaceutical company, the core responsibility is to guide medical strategy and manage clinical staff. Typical roles and responsibilitiesClinical supervision and quality assurance: Ensure that all medical services meet professional and ethical standards. They develop, review, and implement clinical protocols and quality improvement initiatives.Leadership and team management: Provide leadership to medical and clinical teams, including recruiting, hiring, training, and performance evaluation of physicians, nurses, and other medical staff.Strategic planning and policy: Collaborate with senior management to set organizational goals, develop strategic clinical objectives, and establish medical policies.Compliance and regulatory oversight: Monitor and ensure that all medical practices and facility operations comply with federal, state, and local healthcare regulations, such as HIPAA and Joint Commission standards.Financial management: Oversee the medical budget, monitor costs, and ensure efficient resource allocation within the clinical departments.Liaison and communication: Act as a key communicator between medical teams, administrative staff, and external stakeholders, including vendors and partners.Medical expertise and consultation: Offer expert medical advice to staff and act as a clinical resource for complex cases or medical inquiries from patients and families. If you're interested, Kindly forward your resume to:- johnm411411@gmail.com

As a Cardio Care Technician at Erode Medical Centre in Erode, you will play a crucial role in our Cardiology and Ctvs department. You will be responsible for providing support in performing various cardiac diagnostic tests such as ECG, Echo, TMT, and Holter monitoring. Your role will involve preparing patients for cardiac procedures, monitoring vital signs, and cardiac rhythms, as well as maintaining testing equipment. Your compassion and ability to reassure patients will be key in this role. Key Responsibilities: - Assist in performing cardiac diagnostic tests such as ECG, Echo, TMT, and Holter monitoring - Prepare patients for cardiac procedures and explain the process - Monitor and record vital signs and cardiac rhythms - Support cardiologists and nursing staff during cardiac assessments - Maintain testing equipment and ensure proper functionality - Handle patient data and documentation accurately - Ensure safety protocols and infection control standards are followed - Provide compassionate assistance and reassurance to patients Qualifications: - Diploma/Degree in Cardiac Technology, Cardio Care Technology, or related field - Technical knowledge of cardiac diagnostic equipment - Preferred: 2 years of experience in cardiology or cardiac diagnostics - Freshers with a strong interest in cardiology may also apply - Good communication and patient-handling skills - Ability to work in fast-paced clinical settings If you decide to join our team, you will enjoy benefits such as Provident Fund. If you have any further questions, please feel free to reach out to our HR at 7373097135 or email us at emchr2017@gmail.com.,

Role Overview: As a Clinical Research Coordinator (CRC), you will be responsible for managing and coordinating the day-to-day operations of a clinical trial. This includes tasks such as recruiting and screening participants, obtaining informed consent, collecting and managing data, and ensuring compliance with study protocols and regulations. Additionally, you will act as a liaison with sponsors, investigators, and regulatory bodies, maintain meticulous records, and may perform basic clinical procedures. Key Responsibilities: - Manage and coordinate the day-to-day operations of a clinical trial - Recruit and screen participants - Obtain informed consent from participants - Collect and manage data effectively - Ensure compliance with study protocols and regulations - Act as a liaison with sponsors, investigators, and regulatory bodies - Maintain detailed and accurate records - Perform basic clinical procedures as required Qualifications Required: - Bachelor's degree in a relevant field (e.g. life sciences, healthcare) - Strong organizational and communication skills - Attention to detail and ability to maintain accurate records - Knowledge of clinical trial processes and regulations is preferred Please note that the company provides benefits such as a flexible schedule, food provision, health insurance, paid sick time, and Provident Fund. The work location for this role is in person. (Note: Any additional details of the company were not present in the provided job description),

Role Overview: As a caregiver, your role is crucial in providing quality care and support to patients in need. You will play a vital role in assisting patients with personal care tasks, monitoring their health, providing emotional support, assisting with clinical procedures, maintaining supplies and equipment, communicating effectively with healthcare professionals, and ensuring safe patient transportation within the facility. Key Responsibilities: - Patient Care: Assist patients with personal care tasks such as bathing, dressing, feeding, and mobility. - Health Monitoring: Take and record vital signs, report any changes promptly. - Emotional Support: Provide companionship, reassurance, and a listening ear to patients. - Clinical Support: Assist with diagnostic procedures, collect samples, prepare patients for tests. - Communication: Communicate observations and concerns to healthcare professionals. - Supplies and Equipment: Maintain patient care areas, stock supplies, ensure equipment is functioning correctly. - Transportation: Assist with patient transportation within the facility to ensure safety and comfort. Qualifications Required: - Experience in caregiving or a related field would be beneficial. - Basic knowledge of healthcare procedures and protocols. - Strong communication skills and the ability to work well in a team environment. (Note: Omitted additional details of the company mentioned in the job description),

As a full-time on-site Registered Nurse at Krishnagiri, your primary responsibility will be to provide direct patient care, administer medications, collaborate with healthcare professionals, and maintain accurate patient records. You will play a crucial role in monitoring patient conditions, educating individuals on health issues, and ensuring compliance with healthcare regulations. Your key responsibilities will include: - Providing direct patient care - Administering medications - Collaborating with healthcare professionals - Maintaining accurate patient records - Monitoring patient conditions - Educating individuals on health issues - Ensuring compliance with healthcare regulations To excel in this role, you must possess: - Strong clinical skills, including patient assessment and medication administration - Excellent communication and interpersonal skills - Ability to work effectively in a team environment - Attention to detail and organizational skills - Knowledge of healthcare regulations and protocols - Bachelor's degree in Nursing or equivalent - State licensure as a Registered Nurse - CPR certification,

A Clinical Research Associate (CRA) is responsible foroverseeing and coordinating clinical trials to ensure they are conducted safely and effectively, monitoring data collection, ensuring regulatory compliance, and serving as a liaison between study sites, sponsors, and regulatory agencies. Key duties include setting up trials, managing trial supplies, verifying data accuracy, and preparing reports. Core responsibilities    Trial management: Plan, set up, and manage all stages of a clinical trial, from site selection to closing out the study.    Oversight and monitoring: Monitor the trial's execution to ensure it follows the protocol and complies with Good Clinical Practice (GCP) guidelines.    Data integrity: Collect, verify, and manage data to ensure its accuracy and quality.    Site communication: Act as a liaison between the clinical trial sites and the sponsor, ensuring smooth communication and resolving issues.    Regulatory compliance: Ensure all aspects of the trial adhere to relevant regulations and ethical guidelines. Typical duties    Conduct site visits to monitor the progress of the trial.    Verify source data and review trial-related documents, such as informed consent forms.    Manage trial supplies and drug accountability.    Ensure participant safety throughout the trial.    Assist in preparing post-trial reports and publications. 

Job description Management of various solid and hematological malignancies in adult and pediatric patients. Well versed with various front line protocols and routine protocols. For Solid malignancies- Right from diagnostic work up, staging, treatment planning, protocol making, administration of chemotherapy and various targeted agents, to the management of adverse effects, supportive treatment, end of life care, of almost all adult and  tumors. Day care- Institution of chemotherapy and day care procedures. Performing various procedures like Ascetic Tapping, Plural Tapping,  Line Insertion, Central Venous Line Insertion, Lumbar Puncture, Bone Marrow Aspiration and Biopsy for Diagnostic and Therapeutic Purposes. Manage  promised patients with life threatening infections. Well versed with various types of Stem Cell Transplantation Should be well versed with use of Bio safety cabinet for preparation of Chemo drugs. Should be well versed with specialized methods of administering chemotherapy including use of indwelling catheters and chemo ports. Supervise direct patient care of mid-levels and other team members involved in the diagnosis and treatment Should refer patients to Radiotherapy and for surgical treatment whenever necessary. Documentation- Proper documentation of all medical records related to patients according to international standard. Manage and maintain all Medical Oncology patients data base and developing best practical protocol for patients benefit. Working with other doctors as part of a team, either in the same department or within other specialties;

 Leading beauty and wellness brand requires    Senior Wellness   and clinical consultant-- Vellore( Tamil Nadu) One of our client a leading Beauty, wellness and salon brand head-quatered in bangalore operating in over 30 cities in india , today it is one of the fastest growing beauty and wellness brand in india which offers advanced beauty treatments and welness from across its chain of salon outlets. It is over 30 year old brand that brings joy to seeing patrons who have trusted her for over 30 years still turning to her for advice, reaffirming the lasting relationships she has built with passion and expertise. We are looking out for  Senior Wellness and clinical onsultant  for  at Vellore in  Tamil nadu - Client- Leading beauty and wellness brand operation chain of beauty outlets across india - Role- Wellness and Clinical consultant  - Location-   Vellore - Qualification-  Graduate with relevant experience in  medical /aesthetic environment - Experience- Proven experience in a clinic, spa, or medical/aesthetic environment (2+ years preferred). Compensation- competitive - Joining- 0- 15 days THE JD IS AS FOLLOWS Job Summary: We are seeking an experienced and dynamic   Wellness and clinical  Consultant oversee the daily operations of our aesthetic clinic. The ideal candidate will ensure the clinic runs smoothly and efficiently while delivering an exceptional client experience. You will be responsible for staff management, scheduling, inventory control, compliance, marketing support, and overall business development.       Key Responsibilities: Sales Support in implementing promotional campaigns, events, and partnerships.Monitor aesthetic treatment achieving revenue targets.Upsell and cross sales aesthetic services Operations Management Oversee the day-to-day operations of the aesthetic clinic.Ensure a clean, organized, and welcoming environment for clients.Manage appointment scheduling systems and front desk operations.Monitor clinic performance and implement improvements.Staff Management Recruit, train, supervise, and evaluate clinic staff including front desk, aestheticians, and nurses.Organize staff rotas and ensure adequate coverage.Conduct regular team meetings and performance reviews.Customer Service Ensure the highest level of customer satisfaction and handle client complaints professionally.Maintain confidentiality and sensitivity with all patient information.Monitor and improve client feedback and retention metrics.Compliance & Quality Control Ensure compliance with all health, safety, and regulatory requirements.Maintain up-to-date licenses, certifications, and insurance.Enforce standard operating procedures and treatment protocols.Inventory & Supplies Manage inventory levels of skincare products, medical supplies, and clinic materials.Order supplies in a timely and cost-effective manner.Financial Management Assist in managing budgets, billing, invoicing.Prepare financial and operational reports for management.Qualifications: Proven experience in a clinic, spa, or medical/aesthetic environment (2+ years preferred).Strong leadership and people management skills.Excellent organizational and multitasking abilities.Exceptional communication and customer service skills.Understanding of aesthetic treatments, skincare products, and clinic equipment.Proficiency in using clinic management software (e.g., Zenoti, Phorest, or similar).Knowledge of relevant health regulations and standards.   Preferred Qualifications: Certification or training in aesthetics, beauty therapy, or healthcare administration. -Similar experience within the beauty/aesthetic industry. If the position interests you and you find a fitment kindly share your cv and details at career@megmaservices.co.in or contact Rajat- 7011354635 Kindly share the following details - Current ctc and notice period - Expected ctc - Open to work at Vellore - Professional /educational qualification - Relevant experience

As an MBBS doctor interested in technology, AI, and product development, you will play a crucial role in developing AI-driven medical tools for the US healthcare sector. Your responsibilities will include understanding US healthcare workflows, translating clinical logic into requirements for the AI tool, reviewing AI outputs, participating in discussions with the tech team, designing medical content, contributing to quality checks, and continuously learning about US healthcare standards. Key Responsibilities: - Understand US healthcare workflows and guidelines relevant to the product. - Translate clinical logic into requirements/rules/flows for the AI tool. - Review AI outputs for accuracy, safety, and relevance and suggest improvements. - Participate in discussions with the tech team to explain medical concepts clearly. - Help design and review medical content, decision trees, and use cases for the tool. - Contribute to quality checks, test cases, and validation protocols for new features. - Document medical logic, edge cases, and exceptions in a structured, clear manner. - Continuously learn about US healthcare standards, terminology, and best practices. Qualifications Required: - MBBS from a recognized institution. - 0-2 years post-internship experience. - Strong interest in technology, AI, and product-building, not just clinical practice. - Good proficiency in English (written and spoken) - comfortable in documentation, emails, and discussions. Additionally, you must possess the following skills and attributes: - Quick learner with shrewd judgment and strong common sense. - Comfortable asking questions, challenging assumptions, and suggesting improvements. - Detail-oriented with a focus on quality and patient safety, even in a non-clinical role. - Comfortable working in a structured office environment with cross-functional teams. - Basic familiarity or willingness to learn about US medical terms, EHR/EMR, etc. If you are looking for a role that combines your medical expertise with technology and product development, this opportunity offers a gross salary of Rs.35,000/- per month.,

As a Clinical Research Coordinator, your role is crucial in managing and supporting clinical research studies. You will be responsible for coordinating protocols, overseeing data collection, assisting investigators, and ensuring regulatory compliance. By working closely with research staff and participants, you will ensure the smooth day-to-day operations and successful execution of studies. Key Responsibilities: - Plan and coordinate the initiation of research study protocols, ensuring adherence to operating policies and procedures. - Implement and maintain data collection and analysis systems to support research protocols. - Coordinate research subjects and/or volunteers based on specific study objectives. - Ensure efficient day-to-day operation of research and data collection activities. - Coordinate activities of technical support staff and provide support services to investigators and researchers. - Monitor research progress, maintain records, and prepare reports as required. - Participate in clinical floor activities to ensure adequate clinical support for trial activities. - Perform any miscellaneous job-related duties as assigned. Qualifications Required: - B. Pharm, M. Pharm, Pharm. D, M.Sc(Life Sciences), B. Tech (Biotechnology), M.Teh (Biotechnology), B.Sc(Nursing), M.Sc(Nursing), MSc.Microbiology, MSc.Zoology - Fluent English Communication In addition, this opportunity offers benefits such as hostel facilities for female candidates, leave encashment, paid sick time, and ESI coverage. The work schedule is set for day shifts from 9.00 AM to 6.00 PM. Female candidates are preferred, and both freshers and candidates with up to 2 years of experience are welcome to apply. If you meet the qualifications and are looking for a dynamic role in clinical research coordination, this position offers a competitive salary range of 15,100.00 - 16,600.00 per month. For further inquiries or to apply for this position, please contact the provided numbers: 8220011154, 9944450888. Please note that this is a full-time, permanent position with benefits including leave encashment, paid sick time, and Provident Fund. The job requires a Master's degree and in-person work at the specified location.,

As a Functional Testing and User Acceptance Testing expert for Clinical Study databases at Medtronic, your role involves supporting clinical studies and ensuring the accuracy and completeness of study data. You will actively participate in the development and testing of case report forms, study reports, and study databases based on protocol requirements. Your responsibilities will also include managing data discrepancies, processing compensation, coordinating clinical study files, and assisting with audits for completeness and accuracy. Key Responsibilities: - Perform Functional Testing and User Acceptance Testing for Clinical Study databases - Support clinical studies by executing and maintaining data coordination tasks - Verify study data, manage data discrepancies, and ensure timely completion of data forms - Process compensation and identify/resolve compensation discrepancies - Create and manage clinical study files, oversee organization and distribution of study documents - Assist with periodic audits of clinical study files for completeness and accuracy Qualifications Required: - Broad practical knowledge of operational systems and practices - Minimum of 4 years of relevant experience in Functional Testing and User Acceptance Testing - Strong attention to detail and ability to work independently - Excellent communication skills to interact with internal and external stakeholders At Medtronic, you will be part of a global healthcare technology leader that is committed to alleviating pain, restoring health, and extending life. With a team of over 95,000 passionate individuals, we boldly tackle the most challenging health problems facing humanity. Medtronic offers a competitive salary and flexible benefits package, including the Medtronic Incentive Plan (MIP), designed to support you at every career and life stage. Join us in engineering solutions for real people and making a difference in the world. As a Functional Testing and User Acceptance Testing expert for Clinical Study databases at Medtronic, your role involves supporting clinical studies and ensuring the accuracy and completeness of study data. You will actively participate in the development and testing of case report forms, study reports, and study databases based on protocol requirements. Your responsibilities will also include managing data discrepancies, processing compensation, coordinating clinical study files, and assisting with audits for completeness and accuracy. Key Responsibilities: - Perform Functional Testing and User Acceptance Testing for Clinical Study databases - Support clinical studies by executing and maintaining data coordination tasks - Verify study data, manage data discrepancies, and ensure timely completion of data forms - Process compensation and identify/resolve compensation discrepancies - Create and manage clinical study files, oversee organization and distribution of study documents - Assist with periodic audits of clinical study files for completeness and accuracy Qualifications Required: - Broad practical knowledge of operational systems and practices - Minimum of 4 years of relevant experience in Functional Testing and User Acceptance Testing - Strong attention to detail and ability to work independently - Excellent communication skills to interact with internal and external stakeholders At Medtronic, you will be part of a global healthcare technology leader that is committed to alleviating pain, restoring health, and extending life. With a team of over 95,000 passionate individuals, we boldly tackle the most challenging health problems facing humanity. Medtronic offers a competitive salary and flexible benefits package, including the Medtronic Incentive Plan (MIP), designed to support you at every career and life stage. Join us in engineering solutions for real people and making a difference in the world.

You are an experienced professional individual contributor in the Medical Affairs Sub-Function, working under limited supervision. You apply your subject matter knowledge to oversee direction, planning, execution, clinical trials/research, and data collection activities. Your key responsibilities include: - Possessing well-developed skills in overseeing clinical trials/research activities - Contributing to the implementation of clinical protocols and facilitating final reports - Recruiting clinical investigators, negotiating study design and costs - Directing human clinical trials, phases III & IV for company products under development - Participating in adverse event reporting and safety responsibilities monitoring - Coordinating and providing reporting information for regulatory agencies - Monitoring adherence to protocols and determining study completion - Coordinating and overseeing investigator initiations and group studies - Acting as a consultant/liaison with other corporations under licensing agreements Your qualifications include: - Education: Associates Degree in a relevant field - Experience: Minimum 1 year of experience in a similar role,

Role Overview: As a member of the Pharmaceutical & Life Sciences team, your role will involve overseeing the collection, validation, and processing of clinical trial data. You will be responsible for developing and implementing data management procedures for clinical trials, as well as supporting and facilitating the review of medical coding for validity and completeness. Your key focus will be on ensuring compliance with applicable regulations, protocols, and standard operating procedures in India. It will be essential for you to maintain the highest data quality standards throughout the data lifecycle, from data collection to database lock. Additionally, staying updated on industry best practices, technological advancements, and regulatory requirements related to clinical data management will be a crucial part of your responsibilities. Key Responsibilities: - Oversee the collection, validation, and processing of clinical trial data. - Develop and implement data management procedures for clinical trials. - Support and facilitate the review of medical coding for validity and completeness. - Ensure compliance with applicable regulations, protocols, and standard operating procedures in India. - Maintain the highest data quality standards throughout the data lifecycle. - Stay updated on industry best practices, technological advancements, and regulatory requirements related to clinical data management. Qualification Required: - Certification in clinical data management (like CCDM). - Knowledge of CRF design, MS Project, and analytical capabilities. - Knowledge of CDISC standards and data interchange formats (e.g., SDTM, ADaM). - Familiarity with clinical trial design and basic knowledge of regulatory guidelines (FDA/CFR, ICH/GCP). - Understanding of data privacy and protection regulations (e.g., GDPR). - Effective communication and interpersonal skills to collaborate with other teams.,

As a Clinical Research Physician (MBBS) at TruVita Wellness Inc., you will play a crucial role in clinically validating and enhancing the AI Doctor platform to ensure medical safety, ethical practices, and diagnostic accuracy. Your responsibilities will include: - Reviewing and validating AI-generated diagnostic outputs and treatment recommendations. - Supporting or leading clinical research studies to compare AI Doctor outcomes with human doctor diagnoses. - Designing study protocols, consent forms, and ethics committee submissions in collaboration with the Clinical Research Associate. - Supervising patient enrollment, data collection, and medical safety reporting in clinical validation trials. - Acting as a bridge between product/AI teams and clinical stakeholders to uphold medical accuracy. - Providing continuous feedback to enhance clinical symptom checker, triage flow, and e-prescription algorithms. - Monitoring AI behavior for potential medical errors or ethical concerns. - Participating in IRB/IEC meetings to ensure studies comply with ICMR, GCP, HIPAA, and other standards. - Optionally offering teleconsultations to review and compare AI vs. human diagnosis in real-time. Qualifications: - MBBS from a recognized medical college (mandatory); MD in Internal Medicine / Family Medicine / Pediatrics is a plus. - Valid medical license in India (or US license for international candidates). - 2+ years of clinical experience in primary care, internal medicine, or telemedicine. - Experience in clinical research, digital health, or AI-enabled healthcare systems is preferred. - Understanding of Good Clinical Practice (GCP), clinical validation methods, and regulatory ethics. - Strong interest in health technology, innovation, and improving access to care. - Excellent documentation and communication skills. - Ability to collaborate with AI engineers, UX designers, and non-medical stakeholders. Preferred Skills: - Experience with Electronic Health Records (EHR), symptom checkers, or clinical decision support tools. - Knowledge of HIPAA, ICMR, CDSCO, or FDA regulations. - Ability to interpret data related to patient outcomes and diagnostics (with support from data teams). TruVita Wellness Inc. is dedicated to revolutionizing primary care in India and globally by ethically and clinically validating cutting-edge AI healthcare systems. Join our passionate team and contribute to this mission while enjoying flexible work hours and the potential for growth into a medical leadership role.,

As a Clinical Care specialist, your responsibilities will include: - Diagnosing and managing a wide range of ophthalmic conditions, encompassing medical and surgical disorders. - Performing surgical procedures such as cataract surgery, glaucoma surgery, retinal procedures, and oculoplastic interventions. - Providing outpatient consultations and inpatient care. - Interpreting diagnostic tests such as OCT, fluorescein angiography, and visual fields. In terms of Leadership & Supervision, you will be expected to: - Lead and supervise junior doctors, optometrists, orthoptists, and nursing staff. - Ensure adherence to high standards of clinical care and patient safety. - Engage in clinical governance activities including audits, morbidity & mortality meetings, and case reviews. Your role will also involve Training & Education aspects, where you will: - Teach and mentor medical students, residents, and other healthcare professionals. - Organize and deliver Continuing Medical Education (CME) sessions. Furthermore, in the domain of Research & Development, your responsibilities will include: - Participating in or leading clinical research activities and trials. - Publishing in peer-reviewed journals and presenting findings at conferences. Additionally, you will have Administrative Duties like: - Contributing to the development of clinical protocols and policies. - Attending departmental meetings and participating in strategic planning. Please note that this is a Part-time position with an expectation of 18 hours per week during the Evening shift, and the work location is In person.,

Role Overview: As a Clinical Investigator/Research Associate at GLANIS HOSPITAL, you will be responsible for conducting medical and clinical research projects. Your role will involve designing research protocols and utilizing clinical epidemiology and biostatistics skills effectively. Key Responsibilities: - Conducting medical and clinical research projects - Designing research protocols - Utilizing skills in clinical epidemiology and biostatistics effectively Qualifications Required: - Experience/background in conducting medical/clinical research projects - Proficiency in designing research protocols - Strong knowledge of clinical epidemiology and biostatistics GLANIS HOSPITAL is a 100-bed rural teaching hospital located in A. Thottiapatti, Madurai district, dedicated to providing low-cost, affordable healthcare to the rural population. As an educational and research affiliate of GLANIS HOSPITAL, GLANIS INSTITUTE OF MEDICAL SCIENCES offers opportunities for professional growth and development in the healthcare sector. This position offers opportunities for full-time or part-time engagement as well as a consultant role, with salary, compensation, and incentives commensurate with your credentials and experience. The work location is in person during day shifts. We look forward to welcoming dedicated individuals like you to our team at GLANIS HOSPITAL to contribute to our mission of providing high-quality medical education and training to healthcare professionals while serving the rural community with affordable healthcare services.,

As a Clinical Care professional, you will be responsible for diagnosing and managing a wide range of ophthalmic conditions, including medical and surgical disorders. Your role will involve performing surgical procedures such as cataract surgery, glaucoma surgery, retinal procedures, and oculoplastic interventions. Additionally, you will provide outpatient consultations and inpatient care while interpreting diagnostic tests like OCT, fluorescein angiography, and visual fields. Your leadership and supervision skills will be crucial as you lead and supervise junior doctors, optometrists, orthoptists, and nursing staff. Ensuring high standards of clinical care and patient safety will be a key aspect of your responsibilities. You will also actively participate in clinical governance activities, including audits, morbidity & mortality meetings, and case reviews. In the realm of training and education, you will have the opportunity to teach and mentor medical students, residents, and other healthcare professionals. Organizing and delivering CME (Continuing Medical Education) sessions will be part of your contribution to the growth and development of the healthcare community. Research & Development will be a significant part of your role, where you will participate in or lead clinical research activities and trials. Your findings may be published in peer-reviewed journals, and you will have the chance to present them at conferences, contributing to the advancement of medical knowledge. Additionally, you will be involved in administrative duties, such as contributing to the development of clinical protocols and policies. Attending departmental meetings and engaging in strategic planning will also be part of your responsibilities. Qualifications Required: - Medical degree and relevant board certification - Valid medical license to practice - Experience in ophthalmology, particularly in surgical procedures - Strong leadership and communication skills - Ability to work effectively in a team environment This part-time position requires a commitment of 18 hours per week during the evening shift, with the work location being in person. As a Clinical Care professional, you will be responsible for diagnosing and managing a wide range of ophthalmic conditions, including medical and surgical disorders. Your role will involve performing surgical procedures such as cataract surgery, glaucoma surgery, retinal procedures, and oculoplastic interventions. Additionally, you will provide outpatient consultations and inpatient care while interpreting diagnostic tests like OCT, fluorescein angiography, and visual fields. Your leadership and supervision skills will be crucial as you lead and supervise junior doctors, optometrists, orthoptists, and nursing staff. Ensuring high standards of clinical care and patient safety will be a key aspect of your responsibilities. You will also actively participate in clinical governance activities, including audits, morbidity & mortality meetings, and case reviews. In the realm of training and education, you will have the opportunity to teach and mentor medical students, residents, and other healthcare professionals. Organizing and delivering CME (Continuing Medical Education) sessions will be part of your contribution to the growth and development of the healthcare community. Research & Development will be a significant part of your role, where you will participate in or lead clinical research activities and trials. Your findings may be published in peer-reviewed journals, and you will have the chance to present them at conferences, contributing to the advancement of medical knowledge. Additionally, you will be involved in administrative duties, such as contributing to the development of clinical protocols and policies. Attending departmental meetings and engaging in strategic planning will also be part of your responsibilities. Qualifications Required: - Medical degree and relevant board certification - Valid medical license to practice - Experience in ophthalmology, particularly in surgical procedures - Strong leadership and communication skills - Ability to work effectively in a team environment This part-time position requires a commitment of 18 hours per week during the evening shift, with the work location being in person.

Role Overview: You will be a Registered Nurse (RN) with excellent English communication skills representing SolvEdge's healthcare products and performance metrics to U.S. clients. Your key role will involve presenting data-driven insights to hospital and practice stakeholders, ensuring alignment with industry standards, and supporting performance improvement initiatives. Key Responsibilities: - Present performance metrics and quality improvement data to U.S.-based hospitals and medical practices, demonstrating alignment with industry standards and regulatory requirements. - Clearly explain Patient-Reported Outcome Measures (PROMs) and other patient engagement metrics collected through the SolvEdge platform. - Collaborate with internal product and analytics teams to prepare reports, dashboards, and client presentations. - Provide clinical context and guidance to client teams to help improve patient satisfaction and operational performance. - Participate in client meetings (virtual) across U.S. time zones and respond to clinical-related queries. - Maintain a thorough understanding of healthcare quality measures, patient engagement best practices, and emerging trends. Qualifications & Skills: - Registered Nurse (RN) license valid in India (U.S. license a plus but not required). - Bachelor of Science in Nursing (B.Sc Nursing) or equivalent. - Excellent English communication skillsboth spoken and writtenwith the ability to present confidently to healthcare executives. - Prior experience in healthcare quality, patient engagement, or data presentation is preferred. - Strong analytical abilities and familiarity with healthcare performance metrics (e.g., PROMs, HCAHPS, quality indicators). - Comfort working with software platforms, electronic health records (EHRs), and data dashboards. - Flexible to work in U.S. time zones as needed. What We Offer: - Opportunity to work with cutting-edge healthcare technology serving leading U.S. hospitals and practices. - Collaborative, growth-oriented environment with ongoing learning opportunities. - Competitive compensation and benefits package. Company Details (Omitted in JD): SolvEdge is a premier healthcare performance company specializing in a digital care journey platform that revolutionizes patient engagement and care delivery. With over 18 years of dedicated service in the healthcare industry, SolvEdge partners with Fortune 100 medical device companies and hospitals nationwide to provide innovative healthcare solutions. Note: The additional details about SolvEdge have been omitted from the Job Description as per the given instructions.,

As the Director of Artificial Intelligence at a leading healthcare technology provider, your role will involve identifying and prioritizing high-value AI opportunities across machine learning, generative AI, and intelligent agents. You will lead and mentor cross-functional teams of AI/ML, data, BI, and full-stack engineers, fostering excellence and collaboration. Your responsibilities will also include driving AI solution development, implementing scalable MLOps pipelines for model training, deployment, and monitoring, and integrating AI seamlessly into products and workflows. **Key Responsibilities:** - Identify and prioritize high-value AI opportunities across machine learning, generative AI, and intelligent agents. - Lead and mentor cross-functional teams of AI/ML, data, BI, and full-stack engineers. - Drive AI solution development including LLMs, multimodal systems, predictive models, and agent-based frameworks. - Implement scalable MLOps pipelines for model training, deployment, and monitoring using AWS SageMaker, Docker, and Kubernetes. - Architect and optimize AI infrastructure leveraging AWS (Bedrock, AgentCore) and integrating with Azure ML or GCP as needed. - Integrate AI seamlessly into products and workflows, collaborating with full stack and UI teams for user-centric adoption. - Establish best practices for coding, experimentation, and responsible AI, ensuring fairness, transparency, and performance. - Foster innovation and applied research in emerging technologies such as GenAI, reinforcement learning, and autonomous agents. - Align AI initiatives with product roadmaps and track post-deployment success to ensure measurable business impact. **Qualifications Required:** - Bachelors or masters degree in computer science, Artificial Intelligence, Data Science, or a related discipline. - 10-15 years of progressive experience in AI/ML, with at least 3-5 years in strategic or leadership positions. - Demonstrated track record of designing and deploying AI solutions at scale in production-grade environments. In addition to the above role and responsibilities, the company you will be working for is a healthcare technology and clinical services provider backed by a global investment group. Headquartered in the U.S. with offices in India, the company serves multiple state and federal health agencies, impacting over 140 million beneficiaries nationwide. The core offerings of the company include advanced processing, clinical and provider solutions, and quality and compliance services, powered by proprietary digital platforms. Leveraging AI, ML, and cloud technologies, the organization drives modernization in healthcare delivery and has been recognized by leading business journals and corporate growth associations as one of the fastest-growing private companies.,

Role Overview: You will be a Statistician specializing in Clinical Trials & Predictive Biomarkers based in Chennai. Your primary responsibilities will include designing and analyzing clinical trials, developing predictive biomarker models, performing statistical programming, and interpreting research findings. Collaboration with clinical teams, researchers, and stakeholders is key to ensuring the accuracy and integrity of statistical analyses and outcomes. Key Responsibilities: - Design and implement innovative statistical methodologies for clinical trials, including advanced trial designs like umbrella trials. - Utilize predictive biomarkers to identify patient subgroups for targeted therapeutic strategies. - Optimize drug dosing, timing, and combination regimens through robust statistical modeling and analysis. - Conduct meta-analyses to develop assumptions for clinical trial protocols and statistical plans. - Perform systematic data pulls and benchmarking from various sources to support evidence-based decision-making. - Collaborate with cross-functional teams to align statistical strategies with clinical objectives. - Prepare clear reports and presentations for internal stakeholders and regulatory submissions. Qualifications: - PhD in Statistics, Biostatistics, or a related quantitative field with over five years of experience in clinical research as a statistician/data scientist. - Demonstrated expertise in designing and analyzing clinical trials, preferably in pharmaceutical or biotechnology sectors. - Advanced knowledge in predictive biomarker analysis for subgroup identification. - Proficiency in innovative statistical trial designs, including umbrella trials. - Strong skills in optimizing drug dosing, timing, and combinations using statistical methodologies. - Hands-on experience in meta-analysis and evidence synthesis for clinical research. - Proficient in data extraction and benchmarking from diverse sources. - Excellent communication skills to convey complex statistical concepts to technical and non-technical audiences.,