3,501 Medical Research Jobs in Chengalpattu

 Content Analyst / Medical Analyst Qualifications : M.Sc. (Microbiology / Biotechnology) BHMS, BDS, BAMS, BSMS BPT / MPT Work Mode : Hybrid Location : Mumbai *Job Responsibilities Validate product information for medical and laboratory diagnostics from manufacturer and distributor websites or catalogs. Categorize medical/lab products into appropriate taxonomy groups based on internal classification standards and globally recognized schemas. Attribute products with relevant specifications and features via web-based research. Ensure data accuracy, consistency, and completeness at all times. Maintain and update product information as per supplier changes or internal requirements. Perform quality checks and data validation to ensure high data integrity.

Role Overview: As a Remote Consultant Senior Medical Writer at our company, you will be responsible for writing regulatory clinical documents such as clinical trial reports, investigators brochures, summary documents, and other documents covering interpretation and documentation of clinical data. You should have a Masters Degree in Pharmacy or Medicine with a minimum of 7 to 9 years of experience in Medical Writing. Your expertise in scientific research methods and scientific writing skills will be crucial in this role. Additionally, you must have excellent written and spoken English skills at a professional level, along with a genuine interest in scientific communication. Key Responsibilities: - Write regulatory clinical documents including clinical trial reports, investigators brochures, and summary documents - Interpret and document clinical data effectively - Demonstrate expertise in scientific research methods and scientific writing skills - Ensure all documents meet regulatory requirements and guidelines - Collaborate with cross-functional teams to ensure accuracy and completeness of documents Qualifications Required: - Masters Degree in Pharmacy or Medicine - Minimum 7 to 9 years of experience in Medical Writing - Strong written and spoken English skills at a professional level - Demonstrated expertise in scientific research methods and scientific writing - Genuine interest in scientific communication Please email your resume in pdf or doc format to career@ancillarie.com if you are ready to take on challenges, turn opportunities into success, and aim to excel in your career.,

Role Overview: As an Associate Medical Safety Director, you will be responsible for providing medical expertise on pharmacovigilance services as requested by divisions. You will actively participate in assigned trials and standalone safety projects under the supervision of management or senior medical safety directors. Your primary functions will include performing medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs), composing, editing, and medically reviewing Analyses of Similar Events (AOSE), providing coding review of AEs, representing safety and clinical data findings during client meetings, and offering medical support for reports and assessments. You will also participate in safety monitoring committees, provide medical oversight for label development, attend project and client meetings, ensure timely delivery of medical safety deliverables, and stay updated on industry developments. Key Responsibilities: - Perform medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs) - Compose, edit, and medically review Analyses of Similar Events (AOSE) for expedited cases - Provide coding review of AEs and other medical data listings - Represent safety and clinical data review findings during client meetings - Offer medical support for various reports and assessments - Participate in safety monitoring committees - Provide medical oversight for label development - Attend project meetings and client meetings - Ensure timely delivery of medical safety deliverables - Stay updated on medical-safety-regulatory industry developments Qualifications Required: - Medical degree from an accredited school - Relevant clinical practice experience - Knowledge of regulations related to clinical research and safety - Ability to establish and meet priorities and deadlines - Strong communication skills - Ability to build effective relationships - Valid medical license Additional Details (if present): - The role requires a minimum of 5 years of relevant experience or a medical degree with a minimum of 4 years of clinical trial experience - Advanced knowledge of clinical trial conduct, clinical research regulatory requirements, and good clinical system expertise are essential for this position (Note: The JD does not provide additional details about the company.),

As a Medical Affairs Partner (MAP) at Roche based in Malaysia, you play a crucial role in improving the patient journey and creating value within the ecosystem. Your responsibilities include: - Demonstrating personal purpose in improving the patient journey and creating value within the ecosystem - Collaborating closely with the Patient Journey Partners (PJP) and being a core member of the disease area pod - Communicating the value of Roche's science and products to physicians, investigators, and institutions - Working across borders to contribute to virtual, cross-functional work package teams - Overseeing the patient journey, identifying shared purpose among stakeholders, and co-creating better outcomes for patients - Bringing Roche's expertise, science, and knowledge to the ecosystem - Prioritizing and driving solutions that deliver outcomes faster - Acting as a leader, coach, and mentor, supporting team working and contributing to the learning & development of peers - Ensuring high standards of compliance with both external and internal policies and regulations - Supporting GxP-related activities to ensure quality compliance requirements are adhered to You are expected to possess the following skills and experience: - Self-managed, self-directed, and ready to take on empowerment - Enabler mindset leveraging internal and external networks to create value - Outstanding partnering capabilities such as coaching, consulting, and ability to listen deeply - Deep understanding of patient journey, medical affairs strategies & tactics, and Roches present portfolio and future pipeline - Excellent stakeholder engagement skills including partnering with Therapeutic Area Experts (TAEs) and organizations - Evidence generation skills and experience with medical review of promotional materials - Ability to work efficiently in a cross-functional team and experience in agile ways of working - Proficiency in English is required, fluency in the local language is desired - Trained in GMP and GDP requirements for pharmaceutical In terms of education and expertise, you should have: - Medical degree and/or PHD preferred, bachelor's degree in life sciences required - Minimum of 3 years experience within a Medical Affairs role in Pharmaceutical, Diagnostics, Health Sciences, Biotechnology, or related fields - Experience and expertise in Oncology, specifically HCC and Lung Cancer is preferred At Roche, you will be part of a global team dedicated to advancing science and ensuring everyone has access to healthcare. Together, we strive to deliver life-changing healthcare solutions that make a global impact. Join us in building a healthier future, together. Roche is an Equal Opportunity Employer.,

As a Medical Device CRA II, your role will involve site monitoring and site management for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures. You will be responsible for implementing project plans, leading projects of limited scope, and assuming line management responsibilities as assigned. Additionally, you may act as a Local Project Coordinator or Lead CRA when required. Your key responsibilities will include: - Conducting routine monitoring and closeout of clinical sites - Maintaining study files and liaising with vendors - Ensuring study staff have the necessary materials for patient enrollment - Verifying adherence to informed consent procedures and protocol requirements - Reviewing data for accuracy and completeness - Managing travel expenses efficiently - Preparing trip reports and assisting in project management - Participating in protocol development and writing clinical trial reports - Serving as a contact for clinical trial supplies and other vendors - Recruiting potential investigators and negotiating study budgets - Tracking and following up on Serious Adverse Event (SAE) reporting - Performing CRF review and query resolution - Mentoring and training new employees - Coordinating clinical projects and acting as a local client contact - Performing other duties as assigned by management Qualifications required for this role: - University or college degree in life science or related field - Minimum of 3 years relevant clinical research experience - Thorough knowledge of regulatory requirements and drug development process - Fluent in local office language and English - Clinical monitoring and site management experience - Advanced verbal and written communication skills - Ability to work with minimal supervision - Good computer skills and ability to train and supervise junior staff Preferred qualifications: - Additional experience in medical, clinical, pharmaceutical, or related field - Local project coordination or project management experience In terms of physical demands and work environment, this role will require 60-80% overnight travel. You should be comfortable sitting for extended periods, operating a vehicle, and lifting objects up to 15-20 lbs. Work will be primarily in an office environment with occasional travel to client sites, both domestic and international. If you are a proactive individual with strong organizational skills and a passion for clinical research, this role as a Medical Device CRA II could be a great fit for you. As a Medical Device CRA II, your role will involve site monitoring and site management for clinical studies according to Fortrea and/or Sponsor Standard Operating Procedures. You will be responsible for implementing project plans, leading projects of limited scope, and assuming line management responsibilities as assigned. Additionally, you may act as a Local Project Coordinator or Lead CRA when required. Your key responsibilities will include: - Conducting routine monitoring and closeout of clinical sites - Maintaining study files and liaising with vendors - Ensuring study staff have the necessary materials for patient enrollment - Verifying adherence to informed consent procedures and protocol requirements - Reviewing data for accuracy and completeness - Managing travel expenses efficiently - Preparing trip reports and assisting in project management - Participating in protocol development and writing clinical trial reports - Serving as a contact for clinical trial supplies and other vendors - Recruiting potential investigators and negotiating study budgets - Tracking and following up on Serious Adverse Event (SAE) reporting - Performing CRF review and query resolution - Mentoring and training new employees - Coordinating clinical projects and acting as a local client contact - Performing other duties as assigned by management Qualifications required for this role: - University or college degree in life science or related field - Minimum of 3 years relevant clinical research experience - Thorough knowledge of regulatory requirements and drug development process - Fluent in local office language and English - Clinical monitoring and site management experience - Advanced verbal and written communication skills - Ability to work with minimal supervision - Good computer skills and ability to train and supervise junior staff Preferred qualifications: - Additional experience in medical, clinical, pharmaceutical, or related field - Local project coordination or project management experience In terms of physical demands and work environment, this role will require 60-80% overnight travel. You should be comfortable sitting for extended periods, operating a vehicle, and lifting objects up to 15-20 lbs. Work will be primarily in an office environment with occasional travel to client sites, both domestic and international. If you are a proactive individual with strong organizational skills and a passion for clinical research, thi

Medical Coding is the process of converting patient health information into alpha numeric codes. Coders take medial reports from doctors, which may include a patients condition, the doctors diagnosis, a prescription, and whatever procedures the doctor or healthcare provider performed on the patient, and turn that into a set of codes, which make up a crucial part of the medical claim.   Eligibility: All (UG/PG) Life Science& Paramedical Graduates BDS BPT BHMS BAMS Siddha,Unani,Naturopathy {Dip Bsc Msc} Nursing/GNM {B.E M.E} Biomedical Engineering {B.tech,M.tech}Biotechnology Biochemistry Requirement: Knowledge in Anatomy and Physiology Good communication and interpersonal skills Basic Computer Skills   Benefits Weekly 5 days duty Day shift with Sat and Sun off Food and Cab provided by company Incentives based on performance Starting salary 12k to 25k with increment in 6 months for experienced. Abroad opportunities available Bonus for referring friends Medical expenses covered by company Provident Fund will be provided Gratuity after 5 yrs of work experience.   Job Location: Chennai, Coimbatore, Vellore, Trichy, Cuddalore, Pondi Salem, Erode, Namakkal, Thanjavur, Nagercoil, Theni,DindokalThiruvannamalai, Villupuram, Karur, Tirunelveli,Kanniyakumari Tirupati, Kerala, AP,Tamilnadu,Telangana   Reach Us: HR Lavanya- 9566157632  

Producing medical reports and records, correspondence for Physicians, patient information and other administrative material such as statistics and patient data Reviewing and editing transcriptions for spelling, grammar, clarity and correct medical terminology Maintaining medical files and databases for various records such as medical histories

Medical Scribes responsibilities include collaborating with physicians and performing clerical tasks like printing out lab reports or charting doctors appointments, operating electronic health records, and anticipating the needs of the physician to ensure efficiency in a clinical setting.Ultimately, you are responsible for recording doctors conversations with their patients and assisting them in completing paperwork after each visit. You will be required to fill out summaries of what was discussed during the consultation or treatment session, as well as referral letters sent on behalf of your patients insurer.Responsibilities    Taking notes during patient visits and documenting them in the electronic health records system    Learning about the medical process and using a team approach in patient supervision and documentation    Working with a supervising Physician or Doctor to complete and submit medical records    Communicating with patients and supervising Physicians professionally    Completing all administrative tasks efficiently and helping the Physician take tests and give out medicationRequirements and skills    Proven work experience as a Medical Scribe or similar role    Ability to expertly document patient care and transcribe patient appointments    Assure the accuracy of all documentation and records    Advanced computer skills to transcribe and record information across our network    Keep the privacy of all patient information that you learn throughout your duties    Strong organizational and time management skills    Ability to handle high-pressure situations effectively    Excellent written and verbal communication skills

  Assist in planning, initiation, monitoring, and completion of clinical trials. Conduct site qualification, initiation, routine monitoring, and close-out visits. Ensure all trial activities are conducted according to protocol, SOPs, GCP, and applicable regulatory guidelines. Verify that clinical data is accurate, complete, and verifiable from source documents. Maintain essential documents and track trial progress in the Trial Master File (TMF). Support communication between sponsors, investigators, and site staff. Identify and resolve issues that arise during study conduct. Ensure subject safety and proper reporting of adverse events (AEs/SAEs). Prepare visit reports and follow-up letters as per timelines. Participate in investigator meetings and training sessions.  

  Review patient medical records, physician notes, and diagnostic reports for completeness and accuracy. Assign appropriate ICD-10, CPT, and HCPCS codes based on medical documentation. Ensure coding accuracy to optimize reimbursement and reduce claim denials. Maintain compliance with HIPAA and other healthcare privacy regulations. Collaborate with physicians, nurses, and billing teams to clarify diagnoses or procedures. Verify that coded data supports the medical necessity for insurance purposes. Keep updated with changes in coding guidelines and payer requirements. Participate in audits and implement corrective actions for coding errors. Prepare and submit coding reports and documentation as required.  

A medical researcher's duties include designing and conducting studies, collecting and analyzing data, and publishing findings to improve human health. Key skills include strong analytical and critical thinking, scientific and communication skills, attention to detail, and the ability to work collaboratively in a team A medical researcher's duties include designing and conducting studies, collecting and analyzing data, and publishing findings to improve human health. Key skills include strong analytical and critical thinking, scientific and communication skills, attention to detail, and the ability to work collaboratively in a team A medical researcher's duties include designing and conducting studies, collecting and analyzing data, and publishing findings to improve human health. Key skills include strong analytical and critical thinking, scientific and communication skills, attention to detail, and the ability to work collaboratively in a team A medical researcher's duties include designing and conducting studies, collecting and analyzing data, and publishing findings to improve human health. Key skills include strong analytical and critical thinking, scientific and communication skills, attention to detail, and the ability to work collaboratively in a team A medical researcher's duties include designing and conducting studies, collecting and analyzing data, and publishing findings to improve human health. Key skills include strong analytical and critical thinking, scientific and communication skills, attention to detail, and the ability to work collaboratively in a team

Orthopedic Surgeon Job Responsibilities: Examines, diagnoses, and treats diseases and injuries to the musculoskeletal system. Prescribes course of treatment for patients with injuries, disorders, or malformations and performs required surgery. Conducts and supervises direct patient care, including some non-surgical treatment options. Plans and executes disease prevention and health promotion programs. Exercises command of medical units as provided by law and regulations. Conduct medical research on new injuries or diseases, and conducts, supervises, and participates in medical education and training of other medical personnel. Participates in on-call schedule in a responsive and timely manner. Provides outpatient consultation and hospital consultation services. Maintains CME units based on the requirements of the specifying Board. Maintains historical records by documenting symptoms, medications, and treatment events and writing summaries. Enhances department and organization reputation by accepting ownership for accomplishing new and different requests and exploring opportunities to add value to job accomplishments.

Urgent Requirement: We are hiring Assistant Manager- Medical Services for Pharma Industry, Mumbai location. Position Overview: The Executive/Assistant Manager Medical Services will support the Medical Affairs function by providing scientific, clinical, and medical expertise to internal and external stakeholders. The role involves developing and reviewing medical and scientific content, managing medical information, supporting product launches, ensuring ethical promotion, and supporting regulatory team. Role & key responsibilities: Medical & Scientific Support Provide accurate, balanced, and evidence-based medical information to internal teams and external stakeholders. Support marketing, sales, and regulatory teams with scientific input and clinical insights. Review promotional and non-promotional materials for medical accuracy and compliance with relevant codes (e.g., UCPMP, company SOPs). Contribute to the development of medical strategies for assigned therapeutic areas or products. Training & Internal Collaboration Conduct medical and product training sessions for field force and cross-functional teams. Support the development of training modules and scientific updates on company products and relevant disease areas. Collaborate with Regulatory Affairs, Pharmacovigilance, and Marketing to ensure alignment of medical communications. Clinical & Evidence Generation Activities Support the planning and execution of investigator-initiated studies (IIS), post-marketing surveillance, and clinical research projects. Assist in literature reviews, data analysis, and preparation of scientific publications or CME/New product presentations. Compliance & Governance Ensure all medical activities adhere to ethical, legal, and regulatory standards. Maintain confidentiality and integrity in handling sensitive scientific information. Preferred candidate profile Qualifications and Experience: Education: Pharm (Pharmacology). Experience: 25 years in Medical Affairs / Medical Services / Clinical Research within a pharmaceutical organization. Knowledge: In-depth understanding of clinical data interpretation, medical writing, and regulatory guidelines. Skills: Excellent communication and presentation skills. Ability to work cross-functionally and manage multiple projects. Ability to work cross-functionally and manage multiple projects. Proficiency in MS Office and medical databases (PubMed, Embase, etc. Interested candidate can send their cv to prarthanaw@datrax.in or WhatsApp on 930 717 6557.

Job description  Job Title: Medical Writer Key Responsibilities: Develop and review clinical course material (modules, assessments, case studies, etc.) Simplify complex medical concepts for easy understanding by learners Ensure clinical accuracy, academic integrity, and alignment with learning objectives Work closely with doctors, instructional designers, and SMEs for content validation Update content in line with the latest clinical guidelines and standards Collaborate on Al-assisted tools for content enhancement and automation Qualifications & Requirements: Educational Background: MBBS qualified 0-3 years of experience in medical or academic content writing (freshers welcome) Excellent written English and clinical communication skills Strong understanding of core clinical subjects Ability to translate medical jargon into learner-friendly content

As a Medical Anthropologist Research Associate at Munyongo India Private Limited, your primary role will be to gather and provide specialized knowledge related to cultural, social, and behavioral aspects of health and wellness. You will focus on the dynamics of allopathic medicine, Complementary and Alternative Medicine (CAM), and Treatment Seeking Behavior (TSB) patterns across diverse communities. Your responsibilities will include: - Conducting Ethnographic Research & Community Engagement: Design and execute ethnographic research in diverse settings to understand the dynamics between allopathic medicine and CAM within communities. Engage with communities to collect qualitative data respectfully and meaningfully. - Analyzing Treatment Seeking Behaviors: Utilize specialized methodologies to analyze TSB patterns and identify how cultural, social, and economic factors influence healthcare choices and outcomes. - Collaborating Cross-Functionally: Work closely with engineers, healthcare professionals, and project managers to integrate anthropological insights into the design and development of healthcare solutions. - Disseminating Knowledge: Translate complex research findings into actionable strategies and communicate insights across interdisciplinary teams. Prepare and present reports, publications, and recommendations based on research findings. - Conducting Fieldwork: Plan and execute field studies with flexibility and adaptability in various cultural contexts. Travel frequently to conduct research and engage with study populations directly. **Qualifications Required:** **Mandatory:** - Deep theoretical knowledge of medical anthropology principles, including allopathic medicine and CAM. - Proficiency in qualitative research methodologies, especially as they relate to TSB. Familiarity with ethnographic study design, implementation, and analysis. - Strong cultural sensitivity, with the ability to engage effectively with diverse populations. - Excellent interdisciplinary communication skills, capable of conveying complex anthropological concepts to non-specialists. - High proficiency in spoken and written English. **Preferred:** - Technical proficiency in software and tools for data collection, statistical analysis, and presentation of research findings. At Munyongo India Private Limited, we are an industrial, financial, data, and software engineering company with additional expertise in mathematical modeling and operations research. We believe in the significant role of science, technology, engineering, and mathematics in securing the futures of society and the environment. Our diverse projects require a similar underlying knowledge and capabilities to execute them effectively. Join us to work on exciting projects and build a fulfilling career.,

As a Study Coordinator, your role involves assisting in the design and development of study protocols and case report forms (CRFs). You will be responsible for coordinating the logistics of clinical trials or medical research projects, managing timelines, budgets, and resources for research studies. Key Responsibilities: - Support site selection and initiation for clinical trials - Monitor clinical trial sites to ensure compliance with protocols and regulations - Collect, review, and verify study data for accuracy and completeness - Maintain regulatory documentation and study master files Qualifications Required: - Knowledge of Good Clinical Practice (GCP) and ICH guidelines - Familiarity with regulatory bodies like CDSCO in India and FDA in the US - Experience in assisting with ethics committee/institutional review board (IRB) submissions and communications In addition to the above responsibilities, you will ensure adherence to ethical and regulatory compliance standards, including GCP, ICH guidelines, and laws such as CDSCO in India and FDA in the US. You will also support the preparation of study reports and submissions to regulatory authorities. Please note that this is a full-time position with a day shift schedule and the opportunity for a performance bonus. The work location is in-person. As a Study Coordinator, your role involves assisting in the design and development of study protocols and case report forms (CRFs). You will be responsible for coordinating the logistics of clinical trials or medical research projects, managing timelines, budgets, and resources for research studies. Key Responsibilities: - Support site selection and initiation for clinical trials - Monitor clinical trial sites to ensure compliance with protocols and regulations - Collect, review, and verify study data for accuracy and completeness - Maintain regulatory documentation and study master files Qualifications Required: - Knowledge of Good Clinical Practice (GCP) and ICH guidelines - Familiarity with regulatory bodies like CDSCO in India and FDA in the US - Experience in assisting with ethics committee/institutional review board (IRB) submissions and communications In addition to the above responsibilities, you will ensure adherence to ethical and regulatory compliance standards, including GCP, ICH guidelines, and laws such as CDSCO in India and FDA in the US. You will also support the preparation of study reports and submissions to regulatory authorities. Please note that this is a full-time position with a day shift schedule and the opportunity for a performance bonus. The work location is in-person.

As a Freelance Specialist Medical Writer and Editor at Pepgra, you will play a crucial role in ensuring client satisfaction by producing high-quality research and evidence-based policy documents for publication in esteemed journals and regulatory submissions. Specifically, you will focus on Infectious Diseases, handling a diverse range of disorders such as Eastern Equine Encephalitis, Babesiosis, Anthrax, COVID-19, Hantavirus Pulmonary Syndrome, Typhoid Fever, and Meningitis. Your proficiency in English, preferably as a first language from regions like the USA, Europe, or the UK, will be essential for collaborating on clinical research, writing, and editing services. **Role Overview:** - Scientific research and writing in Infectious Diseases, including editing, proofreading, and peer-reviewing various types of manuscripts and documents - Adhering to job-specific instructions and working within set deadlines - Conducting industry-related research and delivering plagiarism-free content - Ensuring correctness in content, terminology, flow, transition, and coherence **Key Responsibilities:** - Hold a Post Doc/PhD/Master's degree or have expertise in Infectious Diseases - Possess research/writing experience and preferably certifications in academic writing, editing, and publishing - Familiarity with academic and scientific writing styles and conventions - Excellent writing, editing skills, and attention to detail **Qualifications Required:** - Post Doc/PhD/Master's degree in Infectious Diseases - Experience in research and writing, with certifications in academic writing, editing, and publishing - Knowledge of academic and scientific writing styles - Excellent writing and editing skills with attention to detail Pepgra offers a great opportunity for you to enhance your skills in research writing and editing while gaining insights into the latest industry trends and writing tips through our learning platform. You will also gain valuable exposure to global research initiatives, making this role a rewarding experience for your professional development.,

Role Overview: As a Clinical Research Assistant at Sarin Skin Solutions, located in Defence Colony, you will be responsible for managing and coordinating clinical research activities. Your main tasks will include collecting and analyzing data, ensuring compliance with regulatory protocols, and assisting in the preparation of research reports. Additionally, you will play a vital role in maintaining accurate records, collaborating with team members, and contributing to the success of research projects. Key Responsibilities: - Manage and coordinate clinical research activities - Collect and analyze data - Ensure adherence to regulatory protocols - Assist in preparing research reports - Maintain accurate records - Collaborate with team members - Contribute to the overall success of research projects Qualifications: - Strong communication and interpersonal skills - Proficiency in medical terminology and research methodologies - Experience with laboratory techniques and procedures - Attention to detail and organizational skills - Ability to handle multiple tasks - Prior experience in clinical research or healthcare setting is an advantage - Bachelor's degree in a relevant field such as biology, healthcare, or medical sciences,

As a Medical Officer in the Medical Services department, your role is to support the execution of medical and occupational health services to ensure healthy and safe operations at the site, following established medical policies and guidelines. **Key Responsibilities:** - Follow all medical and occupational health policies, processes, and standard operating procedures to deliver services consistently and effectively - Implement initiatives and projects to improve medical service processes and best practices - Ensure compliance with safety, infection control, and emergency policies and procedures at all locations - Stay updated with leading practices, research studies, and trends to contribute to continuous improvement of systems and procedures - Manage the occupational health centre and perform administrative duties as per guidelines - Conduct medical monitoring, provide routine/emergency treatment, and maintain a regular supply of medicines at medical centres - Guide patients to avail social security benefits and other entitlements as per organizational and regulatory standards - Conduct Occupational Health awareness programs, workshops, and Industrial Hygiene services - Assist in major health incident investigations, audits, and legal queries for occupational health management - Support in maintaining employee health records and databases as per guidelines and statutory regulations **Qualifications Required:** - Bachelor in Medicine, Bachelor in Surgery (MBBS) - Postgraduate degree or diploma - Occupational Health Courses (AFIH, CIH, DIH) If there are any additional details about the company provided in the job description, please provide that information so it can be included in the final job description.,

As a Clinical Research Medical Advisor (CRMA) at Novartis Healthcare Private Limited in Mumbai, you will play a crucial role in overseeing all clinical or medical aspects associated with Development and prioritized Research programs/trials. Your responsibilities will include providing clinical strategic and tactical leadership, ensuring clinical trial implementation optimization, and maintaining safety standards and clinical data quality. Key Responsibilities: - Provide expertise in clinical development and indications specific to the country/cluster. - Validate study designs and make final decisions on clinical/medical trial feasibility. - Contribute to the scientific/clinical/medical aspects during the start-up phase for fast clinical trial site initiation. - Offer clinical/medical expertise to the clinical trial operations team members and sites for IRB/EC interactions. - Develop clinical/medical trial plans for successful trial implementation. - Conduct comprehensive indication, compound, and protocol training for the clinical operations team and external stakeholders. - Support and collaborate with internal stakeholders on clinical trials. Qualifications Required: - Scientific degree MD/M.B.B.S. - Ability to manage a study from a scientific/medical/clinical perspective. - Demonstrated capability in problem-solving and mediating complex issues. - Effective leadership and communication skills. - Agility to work across different therapeutic areas and indications quickly. - Ideally, 3 years of clinical development experience in the pharmaceutical industry or clinical practice. - Sound understanding of the overall clinical development process and ICH/GCP principles. Join Novartis to contribute to our purpose of reimagining medicine to improve and extend people's lives, aiming to become the most valued and trusted medicines company globally. Be a part of our diverse and inclusive work environment, driving breakthroughs that change patients" lives. Learn more about Novartis and our career opportunities by joining our Novartis Network. Please refer to the Novartis Life Handbook to explore the benefits and rewards we offer to our associates. Additionally, Novartis is committed to providing reasonable accommodations to individuals with disabilities. If you require assistance during the recruitment process or while performing essential job functions, please contact us at [email protected] with your request and contact information, mentioning the job requisition number. Be a part of the Novartis community and contribute to creating a brighter future together. Visit our website to learn more about our commitment to diversity and inclusion and how you can join our mission of helping people with diseases and their families. Location: Mumbai (Head Office) Division: Development Business Unit: Innovative Medicines Functional Area: Research & Development Job Type: Full time Employment Type: Regular Shift Work: No,