Lead Clinical Project Manager

An excellent opportunity has arisen for Lead Clinical Project Manager to join a small Oncology start up in the UK. The post holder will be well-versed in the host of activities that underpin a clinical study, and actively communicate status, obstacles, and issue resolution to the program team.

Job Responsibilities

The post holder will be expected to participate in many activities include site activation, patient enrolment, investigator meetings, data management, and study drug supply, among others.

Support the study team to execute the clinical study in accordance with the clinical development plan/strategy and timelines

Assist in the oversight of activities at the CRO and other clinical vendors; monitor status and provide real-time updates to program team

Lead or assist in:

Contracting and activation of study sitesPreparation and submission of IRB/EC packagesPlanning and conduct of investigator meetingsCoordination of study drug and study suppliesManagement of patient sample collection, archival, and distribution to vendorsCollection or preparation of study-related documentsMay perform periodic visits to sites and/or CROs to assess progress of studies/protocol compliance

Skills and Requirements

Bachelor's or Master's degreeSubstantial, proven experience as a Clinical Project LeadTherapeutic area experience in early phase oncology and immuno-oncologyContract Research Organization (CRO) backgroundStrong problem solving, organizational and time management skills. Ability to multi-task and attend to detail

To Apply

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

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