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Medical Receptionist
You will facilitate quality patient care by managing essential clinical operations.
Tiempo completo
USD7/hora
~USD7 - 7/hora
Negociable
Remoto
Associate Director, Regulatory Affairs - CMC
You will accelerate life-changing therapies by leading global regulatory CMC strategy.
Tiempo completo
Remoto
Clinical Research Associate I (CRA I) / Klinischer Monitor – Full-Time or Part-Time Available (M/W/D)
You will advance life-changing therapies by ensuring clinical trial excellence and data integrity.
Tiempo completo
Remoto
Regulatory Affairs Specialist/Spécialiste Affaires Réglementaires-Canada
You will drive clinical trial success by leading complex regulatory submissions and strategies.
Tiempo completo
Remoto
R
Freelance Clinical Research Associate (France)
You will advance clinical research integrity by driving high-quality site management and compliance.
Tiempo completo
Remoto
Clinical Research Associate - Start Up - Cross TA
You will accelerate clinical trial success by driving site activation and research excellence.
Tiempo completo
Remoto
Senior Regulatory Affairs Program Lead (OTTAVA) - MedTech Surgery
You will advance surgical innovation by leading regulatory strategies for robotic technologies.
Tiempo completo
Remoto
Clinical Research Associate
You will advance clinical innovation by managing diverse trials in a remote environment.
Tiempo completo
Remoto
VP, Research & Clinical Affairs
You will accelerate life-changing HHT therapies by leading global clinical trial operations.
Tiempo completo
Remoto
Associate Director, Regulatory Affairs
You will accelerate global clinical development by leading critical regulatory strategy.
Tiempo completo
Remoto
A
Drug Safety Project and Account Manager
You will advance patient safety by leading global drug safety projects and client partnerships.
Tiempo completo
Remoto
A
Regulatory Affairs Specialist - Manager (FSP)
You will accelerate patient access to innovation by navigating complex regulatory landscapes.
Tiempo completo
Remoto
Senior Manager, Pharmacovigilance Document Management Oversight
You will lead global safety reporting to deliver life-changing therapies to patients worldwide.
Tiempo completo
Remoto
Associate Director, Drug Safety Physician, Medical Review
You will safeguard patient health by leading global medical safety assessments and innovation.
Tiempo completo
Remoto
Pharmacovigilance and Patient Safety Associate
You will advance life-changing therapies by ensuring patient safety in global clinical trials.
Tiempo completo
Remoto
A
Clinical Research Associate in Finland
You will accelerate life-saving treatments by ensuring clinical trial integrity and patient safety.
Tiempo completo
Remoto
P
Contract Specialist, Clinical Research
You will advance clinical research by managing critical agreements and mitigating operational risk.
Tiempo completo
Remoto
Associate Director, Global Regulatory Affairs - GI & Inflammation
You will lead global regulatory strategies to advance complex pharmaceutical development programs.
Tiempo completo
Remoto
Senior Drug Safety Specialist
You will advance global patient safety by leading complex clinical research and pharmacovigilance.
Tiempo completo
Remoto
Clinical Trial Coordinator - Finance - FSP
You will advance clinical research by managing complex trial operations and site budgets.
Tiempo completo
Remoto