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Sr Ctm (Clinical Trial Medical Advisors)

Syneos Health
Syneos Health
2+ years
Not Disclosed
Remote
10 March 19, 2026
Job Description
Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior CTM (Clinical Trial Medical Advisor) | Clinical Trial Science Liaison (CTSL) – Neuroscience/Psychiatry

Location: India (Remote / Field-Based)
Company: Syneos Health
Employment Type: Full-Time (Talent Pipeline Opportunity)

Job Overview
Syneos Health is building a talent pipeline for Senior CTM (Clinical Trial Medical Advisor), a field-based Clinical Trial Science Liaison (CTSL) role within Clinical Development. This position serves as a scientific bridge between clinical trial sites and internal study teams, ensuring high-quality protocol execution, investigator engagement, and data integrity. The role focuses on strengthening scientific communication, supporting trial feasibility, and enhancing study delivery through Risk-Based Quality Management (RBQM) principles.

Key Responsibilities

Scientific Investigator Engagement

  • Build and maintain strong, compliant relationships with Principal Investigators (PIs), Sub-Investigators, and study physicians

  • Provide scientific support on study protocols, endpoints, eligibility criteria, and assessments

  • Facilitate high-quality scientific exchange aligned with governance and compliance standards

Protocol Implementation & Quality Support

  • Reinforce understanding of critical-to-quality protocol elements including endpoints, safety assessments, and procedures

  • Identify common protocol execution challenges and communicate insights to internal teams

  • Support resolution of scientific and operational issues at site level

Trial Feasibility, Enrollment & Retention

  • Provide scientific input on patient recruitment strategies, referral pathways, and enrollment challenges

  • Analyze investigator feedback on patient flow, competing trials, and standard-of-care trends

  • Collaborate with operational teams to enhance recruitment and retention strategies

Clinical Insights & Strategy Contribution

  • Capture and synthesize investigator insights related to protocol feasibility and execution

  • Provide actionable feedback to clinical development teams for protocol optimization

  • Support continuous improvement in study design and implementation

Study Support & Scientific Communication

  • Contribute to investigator meetings, site engagement activities, and scientific presentations

  • Deliver protocol deep-dives and endpoint rationale presentations when required

  • Participate in scientific conferences and clinical meetings to stay updated on therapeutic trends

Compliance & Documentation

  • Ensure all activities comply with ICH-GCP, SOPs, and regulatory requirements

  • Maintain accurate documentation of field interactions, insights, and follow-ups

  • Report adverse events, safety concerns, and protocol risks in a timely manner

Required Qualifications

  • Advanced degree preferred: MD, PharmD, PhD, or equivalent in Life Sciences/Clinical field

  • Strong understanding of clinical trial methodology, GCP, and regulatory frameworks

  • Expertise in Neuroscience or Psychiatry therapeutic areas preferred

Experience Required

  • Minimum 2+ years of relevant experience in clinical research, clinical development, or medical affairs

  • Proven experience engaging with investigators and conducting scientific discussions

  • Experience supporting clinical trial activities and protocol implementation

  • Field-based experience in a CRO, pharmaceutical, or biotech environment is preferred

Key Skills

  • Clinical Trial Science Liaison (CTSL) Expertise

  • Investigator Engagement & Scientific Communication

  • Protocol Interpretation & Execution Support

  • Risk-Based Monitoring & Quality Management

  • Clinical Data Interpretation & Insights Generation

  • Stakeholder Management & Cross-Functional Collaboration

  • Presentation & Scientific Storytelling

Why Join Syneos Health?

  • Be part of a globally recognized biopharmaceutical solutions organization

  • Work on innovative, patient-centric clinical development programs

  • Engage with leading investigators and key opinion leaders globally

  • Access continuous learning, career development, and leadership opportunities

  • Inclusive, diverse, and collaborative work culture

About Syneos Health
Syneos Health is a leading integrated biopharmaceutical solutions organization combining clinical, medical affairs, and commercial expertise to accelerate the delivery of therapies worldwide. With a presence in over 100 countries, Syneos Health is committed to transforming clinical development and improving patient outcomes globally.

Additional Information

  • This is a pipeline opportunity for future hiring needs and may not represent an immediate vacancy

  • Role is primarily field-based with travel requirements based on study and territory needs

How to Apply
Interested candidates can register their interest through Syneos Health’s careers portal or submit their updated resume via ThePharmaDaily.com to stay informed about upcoming opportunities in clinical development and medical affairs.