Senior Clinical Trial Manager – Clinical Research Medical Advisor, M.D / PhD

🔥 15 hours ago

🇸🇰 Slovakia – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 10%

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Syneos Health

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.

📋 Description

• Provide medical and scientific leadership for high-quality execution of clinical trials and studies in the assigned country or cluster • Lead local clinical/medical aspects of trial implementation, including protocol review, site selection support, feasibility assessments, and recruitment strategy planning • Act as medical representative for study design, regulatory interactions, site training, protocol adherence, and patient safety • Identify recruitment and operational challenges and develop mitigation plans • Provide protocol, compound, and indication training to internal and external partners • Provide medical input for informed consent forms and safety reporting • Partner with clinical operations, regulatory, medical affairs, and external experts to optimize trial execution • Review serious adverse events, provide pharmacovigilance support, and ensure clinical data quality • Validate study feasibility and support site engagement and training during early trial start-up • Ensure adherence to Good Clinical Practice, ICH guidelines, and country regulations • Contribute to scientific discussions, advisory boards, and investigator meetings • Provide clinical/medical expertise for regulatory inspections, audits, and trial documentation • May work cross-country

🎯 Requirements

• Advanced scientific degree: M.D., Ph.D., or Pharm.D. (M.D. preferred); subspecialty training desirable • Local Language fluency 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 • Up to 50% travel

🏖️ Benefits

• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition • Total rewards program • Inclusive culture • Reasonable accommodations when appropriate