Clinical Operations Project Manager

Date posted: Jun 24, 2025

City: Rio de Janeiro

Country/Region: BR

Type of Contract: Local Assignement

Job Requisition ID: 8987

Clinical Operations Project Manager

Transform your future with a career in one of the largest multinationals in the pharmaceutical sector!

At our company, we believe that success starts with taking care of people and the world around us. We value commitment, because we know that in order to achieve great results, it is essential to commit in order to succeed. Here, growing is a journey we take by sharing knowledge, experiences and achievements, always with the courage to dare to innovate.

If you identify with our values and want to be part of a team that makes a difference, join us!

Mission

Responsible for running of one or more clinical trial(s) in the assigned countries, ensuring compliance with regulations, Good Clinical Practice, company’s Standard Operational Procedures and technical protocol, and in line with defined study objectives, timelines and budget.

Activities & Responsibilities

• Collaborate to Study Country Prospections;
• Conducts feasibility of assigned studies, including country and centres feasibility assessment;
• Manage the local/regional assigned studies;
• Planning, management and oversight of clinical trials activities such as administrative, budget, regulatory, logistics, contracts, training and set-up concerning all study phases (preparation, recruitment, follow-up and closure);
• Ensures performance and compliance with regulations, Good Clinical Practice, and clinical trials applicable guidelines;
• Contributes and assure technical knowledge of the study team;
• Supervises monitoring and management activities performed by subcontractors;
• Support audit and inspection activities and contribute to CAPAs, including leading resolution of issues when appropriate
• Prepares and conducts local and/or regional investigators meetings;
• Identifies, assesses, mitigates and escalates risks or issues, as appropriate.
• Defines resourcing of the assigned studies;
• Could be delegated by ICTR Director to coordinates specific activities (intra or inter business áreas) a/o funcionally manage others activities in the department, including administrative, regulatory or logistic aspects (e.g. vacation approval and travel expenses).
  
  

Whatever your area of expertise, your work within the Servier Group helps advance therapeutic progress for the benefit of patients. You will be part of teams recognized for their scientific excellence and reach your full potential in a professional environment that encourages you to develop yourself. Tailor-made onboarding journeys, mobility opportunities, quality trainings, responsible management, team spirit... All this and more in a workplace focused on your well-being.

At Servier, we are committed to therapeutic progress to serve patient needs. We put the diversity of our employees as a source of richness for the fulfillment of this vocation.