Clinical Scientist

CK Group have a fantastic opportunity for a Clinical Scientist to join an excellent pharmaceutical company on a full-time, contract basis (18 months).

Where:

Anywhere in Europe (Remote, with up to 20% travel- domestic and international)The Role:

The Clinical Scientist will:

• Participate in adjudication committees to monitor patient adverse events.
• Be responsible for oversight and high-quality implementation and closure of the study, ensuring data integrity.
• Participatein vendor oversight focusing on the integration of data and technology in clinical trials.
• In concert with operational staff, acts as a liaison between the company and clinical investigators for overarching scientific guidance and other potentialnon-medical aspects.
• Be responsible for the TA review and sign off on various operational plans
• Be Responsible for scientific input into HA and EC responses
• Lead data visualization (DV) meetings and ensures decisions are documented and communicated internally and externally
• Qualified CS may perform aspects of medical review under supervision of CL or SRP.

Requirements:

• Right to work in the EU is essential.
• PhD in relevant field (neuro, biology, chem, pharmacy,) PharmD or MD degree
• Experience supporting clinical studies (later stage preferred Phase II - III).
• Experience in clinical research/drug development that has exposed the individual to the rigors of human trial conduct with pharmaceuticals, devices, basic clinical practice with the precepts of Good Clinical Practice.

Apply:

For more information, or to apply for this Clinical Scientist position please contact Karen Kangley on 01246 457730 or email KKangley@ckgroup.co.uk. Please quote job reference 56732 in all correspondence.

It is essential that applicants hold entitlement to work in the UK