Clinical Trial Manager

1 What Youll Be Doing

Your job

Job Summary

As a Clinical Trial Manager (CTM) you will join a dynamic and fast-growing team at the forefront of digital and patient-centered clinical research. Reporting to a Clinical Operations Lead (COPL) you will you will ensure the flawless execution of a diverse portfolio including Resilience-sponsored and ISR across several therapeutic areas.

This is a rare opportunity to consolidate your on-the-ground expertise while stepping into broader coordination missions: stakeholder management process structuring regulatory submissions and contractual follow-up. Youll be working in a rigorous yet supportive environment designed for agility innovation and impact. Regular travel expected.

Your daily responsibilities

Clinical Study Oversight

• Coordinate day-to-day operational and logistical activities of clinical studies

• Support planning and follow-up of visits (site selection initiation monitoring close-out)

• Actively contribute to study meetings and track key performance indicators

• Oversee study delivery at site ensuring quality and client satisfaction.

Regulatory & Contractual Coordination

• Assist with regulatory submissions (ethics committees ANSM)

• Monitor contractual workflows: single-site agreements amendments budget annexes

• Liaise with legal clinical and institutional stakeholders to ensure compliance

• Contribute to site budget tracking and payment follow-up in coordination with Finance

Quality & Documentation

• Support the development of tools trackers SOPs and internal templates

• Maintain regulatory documentation and ensure audit-readiness

• Ensure ongoing compliance with GCP Jardé Law ICH guidelines and GDPR

Cross-functional collaboration

• Work closely with Clinical Scientists Biostatistics and Product teams

• Participate in internal alignment meetings and external study governance committees

• Take part in clinical operations initiatives and cross-functional projects

2 What Youll Bring

Youll definitely have

• A degree in life sciences pharmacy clinical research or biomedical engineering

• 2 years of experience in clinical research (CRA site manager or junior project management)

• Professional fluency in both French and English written and spoken

Youre the right person if you

• Are structured rigorous and autonomous with strong prioritization skills

• Thrive in fast-moving cross-functional environments

• Are curious resourceful and an excellent communicator

• Want to grow in an environment where ownership impact and collaboration are key
  

3 Recruitment

Interview 1 (Role understanding & motivation) with Anne-Julie Eve Clinical Operations Lead or Agathe Combes - Clinical Operations Lead

Interview 2 (Clinical Scientist fit) with Bertille Pommier or Emma Touré Cuq Clinical Scientist

Interview 3 (Practical business case & experience deep-dive) with Anne-Julie Eve

Interview 4 (Medic vision & Soft skills) with Charles Ferté CMO

Interview 5 with Emilie Filoni Culture fit

Start Date : as soon as possible

GDPR : Your personal data will be processed for the purposes of recruitment related activities which include setting up and conducting interviews and tests for applicants evaluating and assessing the results thereto and as is otherwise needed in the recruitment and hiring processes. They will be available only for people involved in the process and erased after 2 years of inactivity.

Under GDPR and as Resilience attach great importance to privacy please note that you have the right to request access to your personal data to request that your personal data be rectified or erased. The Data Protection Officer can be contacted at

For more information please check our .

Required Experience:

Manager