439 Medical Investigation jobs in India
Medical Research Associate (Entrylevel)
Posted today
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Job Description
- Assist in the design and development of study protocols and case report forms (CRFs)
- Coordinate the logistics of clinical trials or medical research projects
- Manage timelines, budgets, and resources for research studies
**Site & Data Management**:
- Support site selection and initiation
- 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
**Regulatory & Ethical Compliance**:
- Ensure adherence to Good Clinical Practice (GCP), ICH guidelines, and applicable laws (e.g., CDSCO in India, FDA in the US)
- Assist in ethics committee/institutional review board (IRB) submissions and communications
- Support preparation of study reports and submissions to regulatory authorities
Pay: From ₹10,000.00 per month
Schedule:
- Day shift
Supplemental Pay:
- Performance bonus
Work Location: In person
Clinical Research Medical Advisor
Posted today
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Job Description Summary
#LI-HybridLocation: Mumbai / Hyderabad, India
Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.
About the Role:
As the Clinical Research Medical Advisor (CRMA), your responsibility lies within the development of Global Clinical Trials – this includes medical oversight for all trials, portfolio and/or protocol medical feasibility, scientific engagement of investigators, protocol and TA training for internal and external stakeholders, medical issue or question management, safety review, strategic input in pre-launch planning.
You will drive compliance across all aspects of clinical trials and CRMA related activities. It will be critical to ensure good communication and stakeholder management cross-functionally within the local country organisation as well as between global and regional teams.
Job Description
Key Responsibilities:
- Medical oversight of clinical trials across all stages and contribute to operational trial deliverables, according to timelines, quality/compliance, and performance standards.
- Drive portfolio/trial medical feasibility within the Global Development framework and provide country clinical strategic guidance and proposals in collaboration with Study and Site Operations Team and Medical Affairs Team.
- Identify and propose new sites for clinical trials, analyse capability, assess patient pool and country treatment landscape, and make recommendations for potential trial inclusion.
- Provide robust indication and protocol training to CRAs, CSMs, RSMs and other functions in the country as needed.
- Responsible for medical related education, implementation and compliance to protocol, standards (SOPs) and best practices for clinical development within assigned clinical trial(s) and within clinical program(s), including sharing lessons learned.
- Provide medical expertise to clinical/operational activities for patient eligibility, medical question-management, safety, amendments, etc.
- Collaborate cross-functionally for the early product launch planning process to ensure Global Development trials conducted are aligned with the local country strategy.
- Support medical/clinical team discussions with local regulatory interactions as needed.
Essential Requirements:
- Medical Degree (MD, MBBS).
- Proven experience in medical practice or pharmaceutical industry experience with a background in clinical trials/medical affairs/life sciences/research in all aspects of drug development including clinical research, GCP, and local regulatory requirements.
- Demonstrated experience in managing projects, feasibility conduct and the execution of strategic plans from a medical perspective.
- Outstanding internal and external stakeholder engagement experience.
Commitment to Diversity and Inclusion / EEO paragraph:
Novartis is committed to building an outstanding, inclusive work environment and diverse teams
representative of the patients and communities we serve.
Accessibility and Accommodation:
Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
Skills Desired
Building Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Internal Medicine, Job Description, Medical Information, Organization Skills, Patient Care, Stakeholder Engagement, Tcp/Ip Protocols, Utilization Management (Um)Clinical Research Medical Advisor
Posted today
Job Viewed
Job Description
Job Description Summary
#LI-HybridLocation: Mumbai / Hyderabad, India
Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.
About the Role:
As the Clinical Research Medical Advisor (CRMA), your responsibility lies within the development of Global Clinical Trials – this includes medical oversight for all trials, portfolio and/or protocol medical feasibility, scientific engagement of investigators, protocol and TA training for internal and external stakeholders, medical issue or question management, safety review, strategic input in pre-launch planning.
You will drive compliance across all aspects of clinical trials and CRMA related activities. It will be critical to ensure good communication and stakeholder management cross-functionally within the local country organisation as well as between global and regional teams.
Job Description
Key Responsibilities:
- Medical oversight of clinical trials across all stages and contribute to operational trial deliverables, according to timelines, quality/compliance, and performance standards.
- Drive portfolio/trial medical feasibility within the Global Development framework and provide country clinical strategic guidance and proposals in collaboration with Study and Site Operations Team and Medical Affairs Team.
- Identify and propose new sites for clinical trials, analyse capability, assess patient pool and country treatment landscape, and make recommendations for potential trial inclusion.
- Provide robust indication and protocol training to CRAs, CSMs, RSMs and other functions in the country as needed.
- Responsible for medical related education, implementation and compliance to protocol, standards (SOPs) and best practices for clinical development within assigned clinical trial(s) and within clinical program(s), including sharing lessons learned.
- Provide medical expertise to clinical/operational activities for patient eligibility, medical question-management, safety, amendments, etc.
- Collaborate cross-functionally for the early product launch planning process to ensure Global Development trials conducted are aligned with the local country strategy.
- Support medical/clinical team discussions with local regulatory interactions as needed.
Essential Requirements:
- Medical Degree (MD, MBBS).
- Proven experience in medical practice or pharmaceutical industry experience with a background in clinical trials/medical affairs/life sciences/research in all aspects of drug development including clinical research, GCP, and local regulatory requirements.
- Demonstrated experience in managing projects, feasibility conduct and the execution of strategic plans from a medical perspective.
- Outstanding internal and external stakeholder engagement experience.
Commitment to Diversity and Inclusion / EEO paragraph:
Novartis is committed to building an outstanding, inclusive work environment and diverse teams
representative of the patients and communities we serve.
Accessibility and Accommodation:
Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
Skills Desired
Building Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Internal Medicine, Job Description, Medical Information, Organization Skills, Patient Care, Stakeholder Engagement, Tcp/Ip Protocols, Utilization Management (Um)Clinical research medical advisor
Posted today
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Job Description
Clinical research medical advisor
Posted 5 days ago
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Job Description
Medical Coder Executive/ Pharmacovigilence /Clinical research/ Trainee
Posted today
Job Viewed
Job Description
Job description
Medical Coding is the process of converting Verbal Descriptions into numeric or alpha numeric by using ICD 10-CM, CPT && HCPCS. As per HIPAA rules healthcare providers need efficient Medical Coders.
Qualification & Specifications :
MBBS,BDS,BHMS,BAMS,BSMS,PHARMACYB.Sc/M.Sc (Life Sciences / Biology / Bio Chemistry / Micro Biology / Nursing / Bio Technology), B.P.T, B.E BIOMEDIAL, B.Tech (Biotechnology/Bio Chemistry).
Skills Required:
* Candidates should have Good Communication & Analytical Skills and should be Good at Medical Terminology (Physiology & Anatomy).
Role:
To review US medical records
Initial file review for identifying merits
Subjective review and analysis to identify instances of negligence, factors contributing to it
To review surgical procedures, pre and post-surgical care, nursing home negligence
To prepare medical submissions
To prepare the medical malpractice case
Regards
Vinothini
Coimbatore
Skills Required
Medical Terminology, human anatomy, Physiology, Icd Coding, Hcpcs, cpt coding
Medical Coder Executive/ Pharmacovigilence /Clinical research/ Trainee
Posted today
Job Viewed
Job Description
Medical Coding is the process of converting Verbal Descriptions into numeric or alpha numeric by using ICD 10-CM, CPT && HCPCS. As per HIPAA rules healthcare providers need efficient Medical Coders.
Qualification & Specifications :
MBBS,BDS,BHMS,BAMS,BSMS,PHARMACYB.Sc/M.Sc (Life Sciences / Biology / Bio Chemistry / Micro Biology / Nursing / Bio Technology), B.P.T, B.E BIOMEDIAL, B.Tech (Biotechnology/Bio Chemistry).
2018 -2024 passed out
Skills Required:
* Candidates should have Good Communication & Analytical Skills and should be Good at Medical Terminology (Physiology & Anatomy).
Role:
To review US medical records
Initial file review for identifying merits
Subjective review and analysis to identify instances of negligence, factors contributing to it
To review surgical procedures, pre and post-surgical care, nursing home negligence
To prepare medical submissions
To prepare the medical malpractice case
Regards
Pujitha
+917200052460
Skills Required
Medical Coding, Anatomy, Icd Coding
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Clinical Research Physician
Posted 3 days ago
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Job Description
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
Job Advert Posting
At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives.
Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.
That's our vision. We're driven by it. And we need talented people who share it.
If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry.
**JOB FUNCTIONS/RESPONSIBILITIES:**
+ Serve as medical team leader on assigned projects,
+ Ensure provision of all contracted activities and identification of out of scope activities on projects assigned
+ Medical review of clinical trial data, including review of Laboratory alerts, Electrocardiogram (ECG) alerts, data from eCRF/ EDC (listing review/ Patient profile review), Eligibility review, Identify protocol deviations, coding review and preparation of Medical Monitoring Reports as per requirement
+ Provide all necessary medical support functions as defined by project specific contractual obligations which will include, but not be limited to, the following:
+ Medical information source
+ Ongoing training for project teams in therapeutic areas as requested
+ Review of study documentation (protocol, CRF. etc.)
+ Contribute to investigator meeting presentations
+ Ongoing safety review of individual patient laboratory reports generated by central laboratories
+ CRF safety review
+ Contribute any necessary medical input into integrated clinical and statistical reports
+ Assist in making presentations to potential clients when appropriate
+ Demonstrate a thorough understanding of ICON Standard Operating Procedures (SOPs) and ensure that all activities are conducted in accordance with current SOPs
+ Demonstrate a thorough understanding of applicable regulatory standards in the country where clinical studies are to be conducted and ensure that all activities are conducted in compliance with current regulations
+ Represent ICON Medical Affairs at teleconferences and meetings
+ Liaise with Sponsors regarding medical issues and medical consultation
+ Ensure quality of medical deliverables in accordance with project plans and ICON Standards
+ Keep the person to whom the Clinical Research Physician reports informed of any issues within the department which require attention
**QUALIFICATIONS/EXPERIENCE REQUIRED:**
+ To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions
+ Medical degree and broad based post graduate clinical experience
+ Solid work experience in a relevant role, ability to medically evaluate clinical data, and good analytical skills
+ Proficiency in English, Good oral and written communication skills
+ Ability and willingness to travel on an as-need basis
+ Excellent presentation skills
+ Good computer skills (MS: Outlook, Word, Excel)
Benefits of Working in ICON:
Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent.
We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.
ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
Clinical Research Associate
Posted today
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Job Description
Job Role : Clinical Research Associate - Study Personnel (Toxicology & Efficacy)
Location: Dholka, Gujarat
Job Responsibilities :
1. Request for required no. of animals
2. Observe the study animals for clinical signs, functional observation battery and
mortality
3. Receipt, storage and handling of chemicals, reagents and solutions
4. Dose preparation and dosing of animals via different routs
5. Weighing of animals, feed consumption, body temperature, dermal observations
6. Randomization of study animals
7. Perform pharma-efficacy studies like batch release test i.e., Pyrogen test, Abnormal
toxicity test, Potency assays, nodule test etc.
8. Blood collection, separation and storage of samples
9. Preparation of study reports
10. Conduct of study, data collection, compilation and verification.
11. Collection of sample(s) / Specimen(s).
12. Preparation and verification of report.
13. To participate in Genotoxicity study
14. Data entry from raw data to computer application and further analysis
15. Co-operate during internal, RQA & sponsor audits of study plans, studies, data,
reports etc.
16. To participate in standardization of new toxicity study
17. Ensure proper labeling of containers (test item, samples etc.)
Documentation:
1. To document deviation from SOP or study plan and communicate directly with SD.
2. Recording raw data promptly and accurately and in compliance with Principles of
GLP.
3. Maintenance of internal records as per in-house SOPs and GLP
4. Update and maintain training records
5. Ensuring the availability of various monitoring certificates such as feed, water,
bedding material, health etc.
6. Request for the issuance of controlled / uncontrolled document and maintain the
documentation
7. Prepare / revise the SOPs as and when required in accordance with in-house SOP
8. Archive the documents as per in-house SOPs when applicable
9. Document the deviation from study plan or SOP and report the incident to SD or
HOS.
10. Record the raw data as and when activities are performed, verify the data and
calculation.
11. Results compilation and analysis
Instrument handling and maintenance:
1. Operate the instruments in accordance with respective instrument SOP, monitor
calibration & maintenance of instrumentation in lab
2. Perform the calibration / maintenance of instruments as per in-house SOP
Clinical Research Executive
Posted 3 days ago
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Job Description
Designation: Clinical Research Executive
Department: Clinical Research
Role Overview:
Specialized in pharmaceutical research and competitive intelligence, with expertise in drug development, clinical trial analytics, and regulatory insights — delivering accurate data.
Key Responsibilities:
Conduct secondary research on drugs, mechanisms, targets, and indications; track innovative drug pipelines, regulatory updates, and clinical trials.
Analyze, maintain, and validate pharmaceutical databases with accuracy on key fields such as drug names, MOA, sponsors, molecule types, and trial data.
Monitor developments from regulatory bodies (US FDA, EMA, CDE, etc.), industry reports, patents, and company filings to provide usable and intellectual data.
Prepare weekly/monthly reports, databooks, and dashboards; deliver strategic recommendations on training the team on accurate data capture and address client queries.
Collect and analyze information from trial registries, filtering by condition, intervention, phase, and recruitment status; capture critical study details such as endpoints, design, inclusion/exclusion criteria, and sponsor information.
Identify tool/process gaps, ensure compliance with company guidelines, and support capability building through training and knowledge sharing to enhance team performance.
Key Skills & Competencies
- Strong knowledge of clinical research methodologies, GCP, and regulatory requirements.
- Experience in drug safety and pharmacovigilance reporting.
- Excellent organizational, documentation, and project management skills.
- Strong interpersonal and communication skills to work effectively with internal teams and external stakeholders.
Qualifications & Experience
- Bachelor’s/Master’s degree in Life Sciences, Pharmacy, Nursing, or related field.
- 5–8 years of experience in clinical research and clinical trial management.
- Hands-on experience in managing clinical trial operations and regulatory submissions.
- Prior experience working in CROs, pharmaceutical, or biotechnology companies preferred.