Alternance Chef De Projets Opérations Cliniques H/f
Merck & Co., Inc.
Paris La Défense, France
Knowledge of clinical trial regulatory framework
Eu regulation no 536/2014 compliance
Strong organizational and time management skills
The role involves participating in the preparation and monitoring of Clinical Trial Authorization requests and substantial modifications under EU regulations
Job Summary
The role involves participating in the preparation and monitoring of Clinical Trial Authorization requests and substantial modifications under EU regulations.
Candidates will work closely with international teams, regulatory affairs, and pharmacovigilance departments to manage clinical trial startup activities.
This 12 to 24-month internship offers exposure to all phases of clinical trials from selection to closure within a leading multinational pharmaceutical company.
Matching Summary
The role involves participating in the preparation and monitoring of Clinical Trial Authorization requests and substantial modifications under EU regulations.
Skills & Requirements
Must-have
Knowledge of clinical trial regulatory framework
EU Regulation No 536/2014 compliance
Strong organizational and time management skills
Fluent English written and oral communication
Microsoft Office suite proficiency
Nice-to-have
Curiosity and dynamism for challenges
Teamwork and interpersonal relationship skills
Analytical thinking and autonomy
Interest in cross-functional collaboration
Key Requirements
Current enrollment in Clinical Research training (Bac +4/5)