Company: Syneos Health
Job Location: India (Remote / Work From Home)
Employment Type: Full-Time
Experience Required: Minimum 2 Years Relevant Experience
Therapeutic Area Preference: Neuroscience / Psychiatry
Job Requisition ID: 25106356
About the Company
Syneos Health is a globally recognized biopharmaceutical solutions company focused on accelerating customer success through integrated clinical development, medical affairs, and commercial solutions. Operating across more than 110 countries with over 29,000 professionals worldwide, the organization supports innovative drug development programs and global clinical research initiatives.
The company is known for delivering high-quality clinical trial support, scientific excellence, and patient-focused healthcare solutions while fostering a collaborative and growth-driven work culture.
Job Overview
The Clinical Scientific Advisor will function as a field-based scientific expert supporting clinical development programs and investigator engagement activities. This remote role involves scientific collaboration with Principal Investigators (PIs), study physicians, and cross-functional clinical research teams to ensure protocol compliance, scientific clarity, and high-quality clinical trial execution.
Candidates with prior experience in clinical research, medical affairs, scientific communication, or clinical development within Neuroscience or Psychiatry therapeutic areas are highly preferred.
This is not a fresher-level opportunity.
Key Responsibilities
Scientific Investigator Engagement
Build and maintain strong scientific relationships with Principal Investigators (PIs), Sub-Investigators, and study physicians
Conduct compliant scientific discussions related to clinical trial protocols and study objectives
Provide scientific guidance regarding eligibility criteria, endpoint rationale, safety assessments, and protocol execution
Clinical Trial Scientific Support
Reinforce understanding of critical protocol elements and data quality requirements
Identify recurring protocol implementation challenges and communicate insights to internal study teams
Support scientific troubleshooting for site-level operational or protocol-related concerns
Feasibility, Enrollment & Retention Strategy
Support clinical trial enrollment planning through investigator discussions and patient flow analysis
Provide scientific input regarding referral trends, competing trials, and patient retention barriers
Collaborate with operational teams including CTMs and CRAs for aligned recruitment strategies
Clinical Insights & Development Feedback
Capture investigator feedback on protocol feasibility and endpoint implementation
Share actionable scientific insights to improve training programs and future protocol development
Support amendment recommendations and risk mitigation activities when required
Scientific Meetings & Presentations
Contribute to investigator meetings, protocol deep-dives, and scientific engagement programs
Deliver scientific presentations and support Q&A preparation
Attend relevant scientific congresses and clinical meetings as required
Compliance & Documentation
Ensure adherence to ICH-GCP guidelines, SOPs, and regulatory requirements
Maintain accurate documentation of scientific interactions and field activities
Report adverse events, product complaints, and safety concerns within established timelines
Eligibility Criteria
Educational Qualification
Advanced scientific or clinical degree preferred: MD, PharmD, PhD, NP/PA, or equivalent clinical research background
Experience Required
Minimum 2 years of relevant experience in Clinical Research, Clinical Development, Medical Affairs, or Scientific Advisory roles
Prior Neuroscience or Psychiatry therapeutic area experience preferred
Strong understanding of clinical trial methodology, protocol execution, and GCP compliance
Required Skills
Scientific communication and stakeholder engagement
Clinical trial operations understanding
Protocol interpretation and endpoint knowledge
Investigator relationship management
Strong analytical and presentation abilities
Excellent written and verbal communication skills
Experience with CTMS, eTMF, EDC, or related clinical systems preferred
Work Model & Travel Requirements
Remote / Home-Based role within India
Candidates should be willing to travel to investigator sites and Mumbai office whenever required
Territory-based field engagement responsibilities included
Why Join Syneos Health?
Work with one of the world’s leading clinical research and biopharmaceutical organizations
Exposure to global clinical development programs and FDA/EMA-regulated studies
Opportunity to collaborate with international investigators and clinical experts
Strong career progression, scientific training, and professional development support
Important Note for Applicants
This opportunity is intended for experienced clinical research professionals and is not suitable for freshers. Candidates with prior exposure to Clinical Trials, Medical Affairs, Site Management, Pharmacovigilance, or Scientific Advisory functions will have a competitive advantage.
About Syneos Health Global Impact
Over the last five years, Syneos Health has contributed to:
94% of Novel FDA-Approved Drugs
95% of EMA Authorized Products
200+ Clinical Studies
73,000+ Research Sites
675,000+ Trial Patients Worldwide
Apply for More Global Clinical Research Jobs
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