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)

Positive 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.

Robust 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.

Solid 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.

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) (India)
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