Syneos Health — a global clinical development leader working across 110+ countries — has opened three major clinical research positions in Mumbai. These full-time, office-based roles offer excellent opportunities for experienced CTAs and clinical trial professionals looking to step up in clinical operations, medical affairs support, and study management.

These new openings will attract high-quality candidates across India, so applying early is recommended.

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Available Positions

1. Clinical Operation Specialist (CTA I – Mumbai)

2. Sr. Clinical Operation Specialist (CTA – Medical Affairs / MAP-PSDS – Mumbai)

3. Clinical Trial Manager I (CTM – Mumbai)

All roles are office-based at the client site (Mumbai).

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1. Clinical Operation Specialist (CTA I – Mumbai)

Key Responsibilities

• Manage end-to-end administrative activities for clinical trials from start-up to close-out
• Support vendor setup, study tracking, and data entry in systems like ECLIPSE, eTMF, SAP
• Handle document upload, completeness checks, and master file maintenance
• Arrange importation of investigational product, lab kits, and ECG supplies
• Support translation, printing, study kits, and investigator file preparation
• Assist in EC/HA submissions, amendments, and follow-up
• Support audits, inspections, and CAPA activities
• Manage payments, invoicing, and fund creation

Qualifications

• 2–3 years of experience as a CTA
• Working knowledge of ICH-GCP, local regulations
• Familiarity with CTMS, eTMF, portals (SIP/MyTrials)
• Strong multitasking and documentation skills

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2. Sr. Clinical Operation Specialist (Medical Affairs – MAP/PSDS)

Key Responsibilities

PSDS/MAP Program Management

• Manage PSDS/MAP submissions in GEMS system
• Coordinate approvals with CMR/GMR
• Draft MAP/PSDS agreements and handle onboarding of physicians
• Coordinate with global MAP/PSDS teams for forecasting and supply

Medical Affairs Study Support

• Handle CTRI submissions, QSR documentation, DCGI dossiers
• Manage drug conversion forms and supply chain requirements
• Liaise with CROs and internal stakeholders
• Maintain archival repositories (Subway/NCV folders)

Vendor & Financial Coordination

• Review and process invoices, publication support, and vendor onboarding

Qualifications

• Strong knowledge of Medical Affairs operations, clinical trial documentation, and MAP/PSDS systems
• Experience with regulatory submissions, CTRI, and MA workflows

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3. Clinical Trial Manager I (CTM – Mumbai)

Key Responsibilities

• Lead and coordinate Phase I–IV clinical trials
• Ensure adherence to protocol, GCP, and regulatory guidelines
• Oversee site communication, study timelines, budgeting, and resourcing
• Track study milestones and present updates to stakeholders
• Troubleshoot operational issues and ensure risk mitigation
• Mentor junior team members

Qualifications

• Bachelor’s degree in life sciences
• 3+ years of clinical trial management experience
• Strong project management, communication, and CTMS proficiency
• Knowledge of regional/global clinical research requirements
• CCRP certification preferred

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Benefits of Working with Syneos Health

• Career progression and internal mobility
• Supportive global team culture (“Total Self” culture)
• Exposure to worldwide clinical programs
• Competitive compensation and performance rewards
• Opportunity to work with 94% of FDA-approved novel therapies

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How to Apply

Application Link for CTA I — 25102825

Application Link for Sr. CTA (MA/MAP/PSDS) — 25102667