Clinical Project Management Associate Director

Associate Director, Clinical Project Management (Neurology Biotech)

Our client is a

fast-growing biotechnology company

dedicated to advancing innovative therapies in

neurology

• . As their clinical pipeline rapidly expands, they are seeking an

Associate Director, Clinical Project Management

to lead critical clinical programs through all phases of development.

This position offers the opportunity to join a

dynamic, science-driven team

with a strong culture of collaboration, agility, and impact.

The role may also be offered at

Senior Clinical Project Manager

level if better aligned for someone looking to advance their career.

Provide leadership and oversight of clinical studies from initiation through close-out.

Develop and manage study timelines, budgets, and operational plans in collaboration with cross-functional teams and CROs.

Ensure effective risk management and proactive issue resolution.

Mentor and support Clinical Project Managers and Clinical Trial Managers.

Contribute to process improvements and strategic planning within the clinical operations function.

Life sciences degree or equivalent; Minimum 7–10 years of experience

in clinical project management, including global study oversight.

Strong background in

neurology or CNS indications

highly desirable.

Ability to thrive in a

fast-paced, growing biotech

environment.

An agile and supportive culture where your voice matters and your impact is visible.

Planet Pharma is an American parented Employment Business / Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.

Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.

We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion / belief, sexual orientation or age.