مدير مشروع سريري

Roles and responsibilities

Clements Partners is a leader in connecting top talent with leading pharmaceutical organizations. We are excited to announce an opening for a Clinical Project Manager to join our esteemed client’s team. This fully remote position is open to candidates across the EMEA region, allowing you the flexibility to work from anywhere while making significant contributions to impactful clinical studies.

About the Role:

As a Clinical Project Manager, you will play a crucial role in leading clinical trials and managing all aspects of project execution. You will be responsible for overseeing project timelines, budgets, and resources, ensuring that each study is completed efficiently and effectively. Your leadership will be instrumental in maintaining compliance with Good Clinical Practice (GCP), regulatory, and ethical standards, which are vital to the success of our clinical trials.

You will collaborate with cross-functional teams, including clinical operations, data management, and regulatory affairs, as well as engage with external stakeholders and sponsors. This collaborative approach will help foster an environment of shared knowledge and innovative problem-solving. You will also be tasked with identifying potential risks throughout the trial process and implementing strategic solutions to keep projects on track, ensuring that timelines and objectives are met.

Key Responsibilities:

• Lead clinical trials and manage all aspects of project execution, ensuring adherence to timelines, budgets, and resource allocation.
• Oversee compliance with GCP, regulatory, and ethical standards to guarantee the integrity of clinical studies.
• Collaborate with cross-functional teams and external stakeholders, ensuring clear communication and alignment on project goals.
• Identify risks early in the project lifecycle and develop effective mitigation strategies to address potential challenges.
• Prepare and present project updates and reports to stakeholders, ensuring transparency and maintaining stakeholder engagement throughout the study lifecycle.

Desired candidate profile

Requirements:

To be considered for this role, candidates should have a minimum of 2 years of experience in clinical trial management. A strong knowledge of GCP and regulatory guidelines is essential, as is the ability to navigate the complexities of clinical research. We seek individuals with excellent organizational skills and strong communication abilities, as these will be critical for effective team collaboration and stakeholder management.

This is an exceptional opportunity for a driven professional looking to advance their career in a dynamic and rewarding environment. At Clements Partners, we value talent and dedication, and we are committed to providing our team members with the support they need to succeed.

If you are passionate about clinical research and want to make a difference in the pharmaceutical industry, we encourage you to apply. Join us in advancing healthcare through innovative clinical studies, while enjoying the flexibility of a remote work environment.