Syneos Health

Clinical Research Medical Advisor – Senior PM

Syneos Health

full-time

Posted on:

Location Type: Remote

Location: Remote • 🇳🇱 Netherlands

Visit company website
AI Apply
Apply

Job Level

Senior

Tech Stack

Google Cloud Platform

About the role

  • Provide medical and scientific leadership to ensure high-quality execution of clinical trials
  • Lead local clinical/medical aspects of trial implementation including protocol review and site selection support
  • Act as the medical representative to support study design, regulatory interactions, and site training
  • Identify proactive recruitment challenges or operational challenges and develop migration plans
  • Provide protocol/compound and indication trainings to internal and external partners
  • Support safety oversight: review serious adverse events (SAEs) and ensure clinical data quality
  • Contribute to early trial start-up by validating study feasibility and supporting site engagement and training
  • Ensure adherence to Good Clinical Practice (GCP), ICH guidelines, and country regulations
  • Contribute to internal and external scientific discussions including advisory boards and investigator meetings
  • Provide clinical/medical expertise for regulatory inspections, audits, and trial documentation

Requirements

  • Advanced scientific degree: M.D., Ph.D., or Pharm.D. (M.D. preferred)
  • Fluency in Dutch required
  • Fluent in English (speaking and writing)
  • Minimum 3 years in clinical development or clinical practice in the pharmaceutical or healthcare sector
  • Strong understanding of clinical trial design, implementation, and ICH/GCP principles
  • Proven ability to analyze complex clinical/scientific issues and provide practical solutions
  • Strong communication and leadership skills to work cross-functionally
  • Problem-solving mindset and agility across therapeutic areas
  • Excellent presentation skills in English and local language
  • Strong protocol review and feasibility assessment skills
  • Understanding of safety and regulatory requirements in clinical trials
  • Experience supporting regulatory submissions, audits and inspections
Benefits
  • supportive and engaged line management
  • technical and therapeutic area training
  • peer recognition
  • total rewards program

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard skills
clinical trial designprotocol reviewsite selectionsafety oversightadverse event reviewclinical data qualitystudy feasibility validationregulatory submissionsauditsinspections
Soft skills
communicationleadershipproblem-solvingagilitypresentation skillsanalytical skillscross-functional collaborationtraininginterpersonal skillsstrategic thinking
Certifications
M.D.Ph.D.Pharm.D.