Senior Clinical Trial Manager – Clinical Research Medical Advisor
Syneos Health
full-time
Posted on:
Location Type: Remote
Location: Remote • 🇮🇹 Italy
Visit company websiteJob Level
Senior
Tech Stack
Google Cloud Platform
About the role
- Provide medical and scientific leadership to ensure the high-quality execution of clinical trials and studies
- Lead local clinical/medical aspects of trial implementation, including protocol review and site selection support
- Act as the medical representative to support study design and regulatory interactions
- Identify pro actively recruitment and operational challenges and develop migration plans
- Provide medical input for Informed Consent Forms (ICFs) and safety reporting
- Partner with clinical operations, regulatory, medical affairs, and external experts to optimize trial execution
- 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
- Ensure adherence to Good Clinical Practice (GCP), ICH guidelines, and country regulations
- 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); subspecialty training desirable
- 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
- Fluent in English (speaking and writing)
Benefits
- Career development and progression
- Supportive and engaged line management
- Technical and therapeutic area training
- Peer recognition and 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 reviewsafety reportingregulatory submissionsfeasibility assessmentGood Clinical Practice (GCP)ICH guidelinesclinical data qualitymedical input for Informed Consent Forms (ICFs)analysis of clinical/scientific issues
Soft skills
communication skillsleadership skillsproblem-solving mindsetagilitypresentation skillscross-functional collaborationability to provide practical solutionsstrong interpersonal skillsorganizational skillsproactive approach
Certifications
M.D.Ph.D.Pharm.D.