POSITION OVERVIEW

Parexel is seeking an experienced Clinical Research Medical Advisor (CRMA) to provide clinical strategic and tactical leadership as a Country Clinical Development representative. The ideal candidate will drive clinical trial excellence through medical expertise, strategic planning, and cross-functional collaboration.

REQUIREMENTS

• MD, PhD or PharmD required
• At least 3 years of experience managing studies from the scientific/medical/clinical perspective in clinical research and drug development in a pharma or CRO setting
• Strong understanding of clinical trial protocols and regulatory requirements
• Excellent communication and stakeholder management skills
• Ability to work across multiple countries and in cross-functional teams
• Knowledge of GCP and ICH guidelines

JOB PURPOSE

• Serve as the accountable leader for all country clinical/medical aspects associated with Development and prioritized research programs/trials
• Provide clinical strategic and tactical leadership as the Country Clinical Development representative (may work across several countries)
• Gather, inform, and act on clinical/medical/scientific insights for clinical trial documentation including concept sheets, protocols, and Informed Consent Forms
• Drive identification and involvement of qualified investigators with greatest recruitment potential
• Identify clinical recruitment hurdles and implement solutions to overcome these challenges
• Ensure adherence to safety standards and clinical data quality through general clinical/medical support
• Collaborate with cross-functional teams (clinical trial operations, Medical Affairs, Patient Engagement) to support successful trial allocation, fast start-up, timely recruitment, and early identification of potential delays