06 Aug
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Kolkata Metropolitan Area
06 Aug
The Pharma Daily - Powered by Vigisolvo
Kolkata Metropolitan Area
Job Type: Full Time, Hybrid, Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICH guidelines, ICSR Case Processing, Labelling Assessment, MedDRA Coding, mRS and EQ-5D-5L, Triage of ICSRs, WHO DD Coding
Medical Scientist / Sr Medical Scientist (Hyderabad Location) Company: Syneos Health
Location: Hyderabad, India
Job ID: 25110971
Updated: July 25, 2026
Work Location: Hyderabad Office
Role Type: Medical Data Review / Clinical Development
About Syneos Health Syneos Health® is a leading fully integrated biopharmaceutical solutions organization focused on accelerating customer success across the drug development and commercialization continuum.
The Company Supports:
- Clinical development
- Medical affairs
- Patient-focused healthcare solutions
- Drug development innovation
Syneos Health brings together scientific expertise, clinical operations, and technology to support successful delivery of therapies. Job Summary The Medical Scientist / Sr Medical Scientist partners with Medical Directors to provide clinical and scientific support for early and late-stage clinical development programs.
The Role Focuses On:
- Medical data review
- Clinical trial data quality
- Patient safety monitoring
- Scientific assessment
- Risk identification
- Cross-functional collaboration
Key Responsibilities Medical Planning & Scientific Support
- Work with Medical Directors to develop:
- Medical Management Plans
- Medical Data Review Plans
- Eligibility Review Plans
- Engage with external experts, consultants, and advisors to obtain required medical/scientific input.
- Support scientific integrity and quality of clinical trial data.
Medical Data Review & Analysis
- Perform regular and ad-hoc medical review of:
- Data listings
- Data visualizations
- Clinical study information
- Analyze data to identify
- Safety risks
- Data patterns
- Emerging trends
- Support documentation of medical reviews.
- Assist in
- Patient profile reviews
- Scientific review of study-level data
- Protocol deviation reviews
- Medical Review Summary Reports
Medical Query Management
- Author medical data queries.
- Review query responses.
- Approve query closure in collaboration with Medical Directors.
- Ensure data integrity and appropriate medical assessment.
Clinical Team Collaboration
- Partner with Medical Directors for:
- Medical data review meetings
- Safety review meetings
- Presentation preparation
- Collaborate with
- Clinical Operations
- Data Management
- Drug Safety & Pharmacovigilance
- Project Management teams
- Identify risks related to
- Data integrity
- Subject safety
- Study execution
- Escalate
- Project risks
- Delivery concerns
- Out-of-scope activities
Project & Quality Management
- Manage assigned project scope, objectives, and deliverables.
- Ensure milestones and timelines are achieved.
- Act as a primary interface between:
- Internal teams
- Customers
- Vendors
- Participate in
- Trusted Process meetings
- Internal audits
- External audits
Regulatory & Compliance Responsibilities Maintain compliance with:
- Data privacy guidelines
- International Council for Harmonisation (ICH)
- Good Clinical Practice (GCP)
- Company SOPs
- Work instructions
- Project plans
- Customer-specific procedures
Required Qualifications Education Required Qualifications:
- PhD
- PharmD
- MBBS
Other Acceptable Qualifications:
- MSc in Life Sciences
- DMD/MD or equivalent scientific discipline
Experience Requirements
- Minimum 1 year of relevant experience
- Experience in
- Clinical research
- Medical data review
- Scientific analysis preferred
Required: Technical & Scientific Skills
- Understanding of scientific principles
- Ability to perform medical data analysis
- Knowledge of
- Drug development process
- Clinical trial methodology
- Disease terminology and pathology
- ICH/GCP guidelines
Communication & Professional Skills
- Excellent English communication skills.
- Strong written and verbal communication abilities.
- Excellent time management skills.
- Ability to manage multiple priorities and deadlines.
- Comfortable working in a regulated and dynamic environment.
- Ability to troubleshoot issues and escalate appropriately.
- Strong interpersonal and teamwork skills.
- Ability to collaborate in cross-functional global teams.
Computer Skills Proficiency in:
- Microsoft Office Suite
- Excel spreadsheets
- Presentation tools
- Data review platforms
Preferred Candidate Profile A successful candidate should be:
- Self-driven and adaptable
- Detail-oriented
- Comfortable with changing priorities
- Skilled in scientific review and clinical data interpretation
- Capable of working independently and within multidisciplinary teams
About Syneos Health Syneos Health has supported:
- 94% of Novel FDA Approved Drugs
- 95% of EMA Authorized Products
- 200+ studies across 73,000 sites
- 675,000+ clinical trial patients
The Company Provides Opportunities In:
- Clinical research
- Medical sciences
- Pharmacovigilance
- Drug development
Application Details Position: Medical Scientist / Sr Medical Scientist Location: Hyderabad, India
Qualification: PhD / PharmD / MBBS / MSc Life Sciences
Experience: Minimum 1 year relevant experience
Key Areas: Medical Data Review, Clinical Development, Medical Monitoring Support
Medical Scientist / Sr Medical Scientist (Hyderabad Location) Company: Syneos Health
Location: Hyderabad, India
Job ID: 25110971
Updated: July 25, 2026
Work Location: Hyderabad Office
Role Type: Medical Data Review / Clinical Development The Company Supports:
- Clinical development
- Medical affairs
- Patient-focused healthcare solutions
- Drug development innovation
Syneos Health brings together scientific expertise, clinical operations, and technology to support successful delivery of therapies.
The Role Focuses On:
- Medical data review
- Clinical trial data quality
- Patient safety monitoring
- Scientific assessment
- Risk identification
- Cross-functional collaboration
Key Responsibilities Medical Planning & Scientific Support
- Work with Medical Directors to develop:
- Medical Management Plans
- Medical Data Review Plans
- Eligibility Review Plans
- Engage with external experts, consultants, and advisors to obtain required medical/scientific input.
- Support scientific integrity and quality of clinical trial data.
Medical Data Review & Analysis
- Perform regular and ad-hoc medical review of:
- Data listings
- Data visualizations
- Clinical study information
- Analyze data to identify
- Safety risks
- Data patterns
- Emerging trends
- Support documentation of medical reviews.
- Assist in
- Patient profile reviews
- Scientific review of study-level data
- Protocol deviation reviews
- Medical Review Summary Reports
Medical Query Management
- Author medical data queries.
- Review query responses.
- Approve query closure in collaboration with Medical Directors.
- Ensure data integrity and appropriate medical assessment.
Clinical Team Collaboration
- Partner with Medical Directors for:
- Medical data review meetings
- Safety review meetings
- Presentation preparation
- Collaborate with
- Clinical Operations
- Data Management
- Drug Safety & Pharmacovigilance
- Project Management teams
- Identify risks related to
- Data integrity
- Subject safety
- Study execution
- Escalate
- Project risks
- Delivery concerns
- Out-of-scope activities
Project & Quality Management
- Manage assigned project scope, objectives, and deliverables.
- Ensure milestones and timelines are achieved.
- Act as a primary interface between:
- Internal teams
- Customers
- Vendors
- Participate in
- Trusted Process meetings
- Internal audits
- External audits
Maintain Compliance With:
- Data privacy guidelines
- International Council for Harmonisation (ICH)
- Good Clinical Practice (GCP)
- Company SOPs
- Work instructions
- Project plans
- Customer-specific procedures
Required Qualifications:
- PhD
- PharmD
- MBBS
Other Acceptable Qualifications:
- MSc in Life Sciences
- DMD/MD or equivalent scientific discipline
Experience Requirements
- Minimum 1 year of relevant experience
- Experience in
- Clinical research
- Medical data review
- Scientific analysis preferred
Required:
- Understanding of scientific principles
- Ability to perform medical data analysis
- Knowledge of
- Drug development process
- Clinical trial methodology
- Disease terminology and pathology
- ICH/GCP guidelines
Communication & Professional Skills
- Excellent English communication skills.
- Strong written and verbal communication abilities.
- Excellent time management skills.
- Ability to manage multiple priorities and deadlines.
- Comfortable working in a regulated and agile environment.
- Ability to troubleshoot issues and escalate appropriately.
- Solid interpersonal and teamwork skills.
- Ability to collaborate in cross-functional global teams.
Proficiency In:
- Microsoft Office Suite
- Excel spreadsheets
- Presentation tools
- Data review platforms
A Successful Candidate Should Be:
- Self-driven and adaptable
- Detail-oriented
- Comfortable with changing priorities
- Skilled in scientific review and clinical data interpretation
- Capable of working independently and within multidisciplinary teams
Syneos Health Has Supported:
- 94% of Novel FDA Approved Drugs
- 95% of EMA Authorized Products
- 200+ studies across 73,000 sites
- 675,000+ clinical trial patients
The Company Provides Opportunities In:
- Clinical research
- Medical sciences
- Pharmacovigilance
- Drug development
Application Details Position: Medical Scientist / Sr Medical Scientist Location: Hyderabad, India
Qualification: PhD / PharmD / MBBS / MSc Life Sciences
Experience: Minimum 1 year relevant experience
Key Areas: Medical Data Review, Clinical Development, Medical Monitoring Support
📌 Medical Scientist / Sr Medical Scientist (Hyderabad Location) (Kolkata Metropolitan Area)
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📍 Kolkata Metropolitan Area