Overview

Reference Number: JO-2109-477360
Clinical Scientist
Rate: Negotiable
Job Type: Contract
Location: Cambridge

Clinical Scientist

12-month contract

Cambridge: Hybrid working

450-550 per day DOE

CPL Life Sciences are actively recruiting for an experienced Clinical Scientist to support one of our specialist clients on one or more large scale global Oncology study. This position will be supporting the conduct of clinical trials, ensuring all protocols are met, clinical data oversight and relevant reporting.

This contract will be ideal for an individual seeking a contract in which they can contribute to market leading oncology studies, liaising with the clinical, scientific, and medical team to ensure program targets are achieved.

Key tasks and responsibilities will include:

Providing clinical oversight of late phase clinical studies

Provide scientific and medical support on the clinical trial

Be the key point of contact for clinical sites, health authorities and CROs

Support the generation of clinical study reports

Liaise with the clinical operations team on the implementation of study protocols

Lead the execution of the clinical elements of all relevant documentation

Oversee the clinical study from start up to study reporting

Preparation of key clinical documentation and briefing documents

Contribute to regulatory submissions when required

Cross-functional team communication

Experience required:

Oncology experience is essential

Previous experience on large scale clinical studies

Experience as a Clinical Scientist

Strong communication skills

Proficient with GCP and ICH guidelines

Clinical analysis and reporting

Experience with input or oversight of clinical protocols

If this position if of interest to you as a Clinical Scientist then please apply here or send your CV to sarah.phillips@cpl.com.

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