India Health & medical researchers Jobs – 175 Open Jobs Today

Assoc Medical Safety Dir
IQVIA —Bengaluru, Karnataka
- Full-time
- Remote
- Research
- Bachelor's degree
- Work from home
Research Associate
DIFGEN PHARMACEUTICALS PRIVATE LIMITED —Kukatpally, Hyderabad, Telangana
- ₹8,00,000 a year
- Master's degree
Dir, Medical Safety
IQVIA —Bengaluru, Karnataka
- Full-time
- Remote
- Work from home
Pharmacovigilance Services Associate
Accenture —Bengaluru, Karnataka
- Full-time
- Master's degree
- Bachelor's degree
- Data entry
Pharmacovigilance
Refined Reports Data —Nagpur, Maharashtra
- ₹25,064.34 - ₹35,471.11 a month
- Full-time
- Bachelor's degree
- In-person
- Health insurance
- Paid sick time
Quick apply
5d
Junior Associate - Evidence Synthesis, Clinical Outcome assessments (COA)
Sanofi —Hyderabad, Telangana
- Full-time
- Writing skills
- English
- Analysis skills
TL-Medical Safety
Cognizant —Mumbai, Maharashtra
- Full-time
- Hybrid work
- Research
- Analysis skills
- Travel
- Health insurance
Medical Reviewer
Sitero LLC —Mysuru, Karnataka
- Full-time
- Medicine
- Bachelor's degree
- EMR systems
- Health insurance
- Paid time off
Quick apply
12d
Clinical Research - Infection control
Thermaissance —Mumbai, Maharashtra
- ₹50,000 - ₹70,000 a month
- Part-time
- Medicine
- B.Sc
- Master's degree
Quick apply
1d
Drug Safety Associate
Accenture —Chennai, Tamil Nadu
- Full-time
- B.Sc
- Bachelor's degree
- Data entry
Drug Safety Associate
Statistical Pharma —Pune, Maharashtra
- ₹25,000 - ₹35,000 a month
- Full-time
- Bachelor's degree
- Python
- Health insurance
Quick apply
9d
Research Associate III - Evidence Synthesis
Thermo Fisher Scientific —Remote
- Full-time
- Remote
- Doctoral degree
- Research
- Master's degree
Assay Development Scientist
INVITRONICS MEDTECH PRIVATE LIMITED —Pune, Maharashtra
- ₹3,00,000 - ₹4,00,000 a year
- Full-time
- Doctoral degree
- Laboratory experience
- Master's degree
- Paid sick time
Quick apply
Research Associate - M.Sc Biotech / Life science
NeuroGen Brain and Spine Institute —Navi Mumbai, Maharashtra
- English
- Microsoft Office
- Master's degree
Pharmacovigilance ICSR Intern
Medifodil Smart Pharma Solutions —Hyderabad, Telangana
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
SPE-Pharmacovigilance
Cognizant —Mumbai, Maharashtra
- Full-time
- Hybrid work
- Research
- Analysis skills
- No travel
8d
Drug Safety Associate
Jeevan —Hyderabad, Telangana
Pharmacovigilance Executive
Indian Institute of Patent and Trademark Education and Research —Kolkata, West Bengal
- ₹2,00,000 - ₹4,00,000 a year
- Full-time
- Research
- Master's degree
- Bachelor's degree
Project Research Scientist - II (Non-Medical)
Amity University —Noida, Uttar Pradesh
- ₹67,000 a month
- Email
- Doctoral degree
- Research
- Master's degree
Research Intern, Drug Discovery
Katalyst Healthcares & Life Sciences —Guntur, Andhra Pradesh
- Full-time
- Hybrid work
- B.Sc
- Master's degree
- Bachelor's degree
Quick apply

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Assoc Medical Safety Dir

IQVIA -
Bengaluru, Karnataka

Apply Now

Job details

Full-time

Benefits

Work from home

Qualifications

Clinical research
Research
Bachelor's degree
Clinical trials

Full job description

Bengaluru, India | Full time | Home-based | R1552764

Job Overview
Provide medical expertise on pharmacovigilance services to divisions as requested. The Associate Medical Safety Director participates in all aspects of Medical Safety’s involvement on assigned trials and stand alone safety projects with appropriate oversight from management or more senior medical safety directors.

Essential Functions

Perform medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs) including narrative content, queries, coding, expectedness, seriousness, causality and company summary
Compose, edit and medically review Analyses of Similar Events (AOSE) for expedited cases as appropriate based on regulatory requirements
Serve as an internal consultant to pharmacovigilance case processing teams on projects being supported
Provide aggregate reviews of safety information, including clinical data, to maintain oversight of a product’s safety profile
Provide coding review of AEs, Past medical history, Concomitant medications or other medical data listings to verify and medically vet clinical data
Represent safety and clinical data review findings during client meetings
Provide medical review and edits to IND Annual Reports, EU Periodic Benefit Risk Evaluation Reports, EU Periodic Safety Update Reports, EU Development Safety Update Reports, US Periodic Reports
Provide medical review and edits of Development Risk Management Plans, EU Risk Management Plans or US Risk Evaluation and Mitigation Strategies
Provide medical oversight for label development, review and change
Provide medical support and attendance at Data Safety Monitoring Board Meetings
Attends and contributes medical safety evaluation on Safety Monitoring Committees
Provide medical safety contributions to the Integrated Safety Summary or Common Technical Document
Provide medical review and edits to Drug Safety Reports or other benefit-risk assessments
Review and sign off on both the Project Safety Plan and the Medical Monitoring Plan per medical safety scope agreed in contract
Perform Medical Safety review of the protocol, Investigative Drug Brochure (IDB), and/or Case Report Forms (CRFs) for appropriate safety content and data capture.
Act as Global Safety Physician or Assistant or Back-up on projects as assigned
Attend project meetings, medical safety team meetings, and client meetings as requested
Ensure coverage for all medical safety deliverables within regulatory or contracted timelines
Provide medical escalation support for medical information projects
Provide medical escalation support for EU Qualified Persons for Pharmacovigilance projects
24 hour medical support as required on assigned projects
Maintain awareness of medical-safety-regulatory industry developments

Qualifications

Other A medical degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education Req
Three (3) years of clinical practice experience (e.g graduate medical training) with two (2) additional years in the pharmaceutical or associated industry in any role. Or equivalent combination of education, training and experience Req
Knowledge of applicable federal and local regulations and guidelines pertaining to clinical research including knowledge of regulations and guidelines pertaining to safety and good clinical practice
Knowledge of clinical trials and pharmaceutical research process
Ability to establish and meet priorities, deadlines, and objectives.
Skills in providing consultation and advice on multiple assignments required, as well as initiative and flexibility
Ability to establish and maintain effective working relationships with coworkers, managers and clients
A valid medical license, or equivalent, from the country or region in which he/she resides and works Pref

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Apply Now

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health & medical researchers jobs in india

Assoc Medical Safety Dir

Research Associate

Dir, Medical Safety

Pharmacovigilance Services Associate

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Junior Associate - Evidence Synthesis, Clinical Outcome assessments (COA)

TL-Medical Safety

Medical Reviewer

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Drug Safety Associate

Drug Safety Associate

Research Associate III - Evidence Synthesis

Assay Development Scientist

Research Associate - M.Sc Biotech / Life science

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SPE-Pharmacovigilance

Drug Safety Associate

Pharmacovigilance Executive

Project Research Scientist - II (Non-Medical)

Research Intern, Drug Discovery

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