Clinical Research Manager @Parexel
Medical
Salary unspecified
Remote Location
Employment Type full-time
Posted 2d ago

[Hiring] Clinical Research Manager @Parexel

2d ago - Parexel is hiring a remote Clinical Research Manager. πŸ’Έ Salary: unspecified πŸ“Location: France

Role Description

We are seeking a Clinical Research Manager (CRM) to join our team in a home-based capacity in France. As a Clinical Research Manager, you will play a pivotal role in the successful delivery of complex oncology clinical trials for a top pharmaceutical client.

This position is responsible for the end-to-end management and performance of assigned protocols, ensuring compliance with ICH-GCP, local regulations, client requirements, and quality standards.

Working across study start-up, maintenance, and close-out, you will provide strategic oversight of trial execution, site performance, vendor management, and CRA activities. You will collaborate with cross-functional partners, drive operational excellence, and help ensure that innovative therapies reach patients efficiently and safely.

You will join a fast-paced, growth-oriented environment where your expertise directly contributes to the advancement of life-changing treatments. With exposure to global stakeholders, leadership opportunities, and continuous development, this role offers a strong platform for career progression within clinical research and project leadership.

Key Responsibilities

  • Lead end-to-end performance and project management of assigned clinical trial protocols in compliance with ICH-GCP, local regulations, and client requirements.
  • Manage study start-up activities, including oversight of site selection strategies, monitoring plans, and trial planning tools.
  • Review and contribute to patient recruitment and retention strategies to support study delivery objectives.
  • Provide leadership, guidance, and direction to project team members across multiple locations and functions.
  • Evaluate project resource requirements and monitor resource utilization throughout the study lifecycle.
  • Address and resolve site issues, ensuring timely escalation and successful closure of identified risks.
  • Monitor study timelines, patient recruitment, retention, and data cleaning activities to support successful project outcomes.
  • Maintain oversight of quality standards and ensure appropriate follow-up of quality-related issues.
  • Drive process improvements that enhance study efficiency and operational performance.
  • Contribute to revenue recognition forecasting and project planning activities, as required.
  • Collaborate with project teams on database lock activities and study close-out deliverables.
  • Ensure completion of all administrative close-out procedures, study archiving activities, and client documentation requirements.

Qualifications

  • Strong leadership, stakeholder management, and project coordination skills.
  • Experience working in clinical research, healthcare, or a regulated environment.
  • The ability to collaborate across cross-functional and global teams while communicating effectively with internal and external stakeholders.
  • A patient-focused mindset and commitment to quality, compliance, and operational excellence.
  • Comfort working with clinical trial systems, study management processes, and project planning tools.

Requirements

  • Degree in a life science, nursing qualification, or relevant clinical and/or clinical management experience.
  • Substantial experience in clinical research, including relevant experience as a team leader in clinical functions or proven experience coordinating clinical trials.
  • Knowledge of ICH-GCP, regulatory requirements, SOPs, and clinical trial processes.
  • Experience managing clinical trial activities, study operations, site oversight, and vendor relationships.
  • Strong communication, organization, leadership, negotiation, and problem-solving skills.
  • Strong command of written and spoken English language.

Preferred Qualifications

  • Previous experience as a Clinical Research Associate (CRA).
  • Experience in oncology clinical trials.
  • Experience within a pharmaceutical company, healthcare organization, or contract research organization.
  • Knowledge of project management methodologies and clinical study lifecycle management.

Benefits

  • Medical Plan
  • Life Assurance
  • Pension

We offer a comprehensive benefits package to eligible employees, which includes life assurance and medical plan, and additional benefit offerings in accordance with the terms of our applicable plans.

Before You Apply
️
remote Be aware of the location restriction for this remote position: France
β€Ό Beware of scams! When applying for jobs, you should NEVER have to pay anything. Learn more.
Clinical Research Manager @Parexel
Medical
Salary unspecified
Remote Location
Employment Type full-time
Posted 2d ago
Apply for this position
Did not apply βœ“
Applied βœ“
Sent Follow-Up βœ“
Interview Scheduled βœ“
Interview Completed βœ“
Offer Accepted βœ“
Offer Declined βœ“
Application Denied βœ“
Unlock 130,000+ Remote Jobs
️
remote Be aware of the location restriction for this remote position: France
β€Ό Beware of scams! When applying for jobs, you should NEVER have to pay anything. Learn more.
Apply for this position
Did not apply βœ“
Applied βœ“
Sent Follow-Up βœ“
Interview Scheduled βœ“
Interview Completed βœ“
Offer Accepted βœ“
Offer Declined βœ“
Application Denied βœ“
Unlock 130,000+ Remote Jobs
Γ—
Apply to the best remote jobs
before everyone else

Access 130,000+ vetted remote jobs and get daily alerts.

4.9 β˜…β˜…β˜…β˜…β˜… from 500+ reviews

⚑ 131,421+ remote jobs, refreshed hourly

πŸ”” Real-time alerts: Apply first

πŸ›‘οΈ Vetted companies, no scams, true remote only

Unlock All Jobs Now

Maybe later