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Senior Clinical Study Manager

Cambridgeshire   •  Negotiable  •  Permanent, Full time

Senior Clinical Study Manager


UK Elstree Hybrid 1x a week in office.

Salary: circa 65,000 plus benefits

We have a new opening for an experienced Senior Clinical Study Manager to join a small pharma company. This is an exciting business that deliver life-saving treatments for conditions related to autoimmune deficiencies, bleeding disorders and critical care. You will initially be responsible for study management of one Phase I US based study with key responsibilities around vendor set up and oversight and key document preparation.

Key Responsibilities:

-CRO and Vendor management

-Feasibility and site selection

-Delivery of clinical trial through the full life cycle

-Budget management

-Risk management strategies, quality assurance and audits

-Investigational Medicinal Product (IMP) and Supplies Management

-Prepare/review clinical trial protocols, subject information leaflets/consent forms and Investigator Brochures.

-Mentor clinical research staff and consultants, including the induction and training for new/junior team members.

Key Requirements:

-Minimum 6 years of CSM experience

-Phase I and start up experience

-Strong scientific and/or operational experience

-Vendor management experience, especially with CROs.

-Experience reviewing/preparing key clinical trial documentations protocols, investigator brochures, SOPs, Consent forms.

-Flexible attitude

-Pharma and/or CRO experience

If this role is of interest, please send your CV to hanna.poole@cpl.com or call 0118 952 2793 for more information.

  • Agency: Cpl Life Sciences
  • Contact: Hanna Poole
  • Reference: JO-2111-479888_2
  • Posted: 10th November 2021
  • Expires: 8th December 2021

Cpl Life Sciences

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