Clinical Research Medical Advisor
Core
Shape clinical trial strategy and drive operational excellence to accelerate the development of innovative therapies for patients.
Role type
Senior Clinical Research Medical Advisor (CRMA)
Builds
Clinical development programs and clinical trials
Domain
Pharmaceutical industry, clinical development
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Clinical development expertise, protocol feasibility evaluation, site/Country-specific scientific content management, patient recruitment strategy, ICH/GCP principles knowledge, cross-functional collaboration
Preferred skills
Problem-solving in complex clinical/operational issues, agile mindset
Technologies
None stated
Responsibilities
Validate study designs and make final decisions on clinical trial protocol feasibility; Contribute to scientific aspects of the start-up phase to ensure fast site initiation; Provide expertise for IRB/EC interactions; Decide on Informed Consent Form content and patient language; Interact with external experts (Regulatory Authorities, Medical Experts, Patient Advocacy Groups); Drive patient recruitment strategies and address enrolment/data quality challenges
Seniority
Senior, hands-on IC
