We've got a great role for an oncology project manager, based in London to work at a client's site supporting clinical trials of all phases, but especially early phase oncology.

Summary Of the Clinical Project Manager Position

Responsible for management of multiple assigned projects throughout all lifecycle phases in oncology.

Our client works as an SMO/ CRO so you will need to ensure project work completion to the client expectations, ensuring quality deliverables on time and within budget and in accordance with SOPs, ICH GCP, applicable laws, policies and practices.

You will also act as the principal liaison with clients to ensure effective and timely communication of project progress, issues, and plans for resolution of those issues.

You should be confident enough to provide leadership in the development of clinical trials and related documents.

You will work closely and effectively with cross-functional teams and be expected to manage your CTA, CRA and other team members.

You may also need to provide input in business development proposals and attends bid defenses, so work in SMO or CRO helps with this.

Qualifications

You should have:

• Bachelor's Degree in science
• Previous experience as a Clinical Project Manager for a CRO/ pharma/ biotech company or Academic unit or SMO
• Demonstrated leadership skills
• Experience in oncology clinical research phases I-III

It Would Be Helpful If You Had

• Experience writing clinical protocols and other technical documents
• Prior experience mentoring and/or training less senior team members
• Experience leading study timelines, deliverables, and/or vendors

This is initially to cover maternity, starting in May/ June

Contact Gail Kniveton or Henry Grover for more information

info@pop-science.co.uk

+447971666239