Senior Manager Clinical Operations

London, England
Sep 28, 2021
Required Education
Bachelors Degree
Position Type
Full time

Senior Manager Clinical Operations

Location: London

Reporting to: Associate Director/ Director of Clinical Operations

Job Summary

Reporting to the Associate Director / Director of Clinical Operations, the Sn Clinical Operations Manager will be accountable for managing the clinical operation activities for 2 to 3 clinical studies. This person will be key in driving the clinical studies day to day activities, ensuring on time delivery of main clinical milestones, as well as respect of GCP.

Key Elements and Responsibilities

- Lead, manage and co-ordinate the conduct of assigned clinical trials from study start-up to close out in accordance with ICH-GCP

- Oversees the quality of the clinical operations for the studies he/she is in charge of

- Collaborates with cross functional stakeholders to ensure timely and on budget execution of clinical trial deliverables

o Coordinates medical writing and all the activities necessary for delivering of documentation: publishing, QC, etc

o Manages data management and statisticians ensuring data base maintenance, interim and final database locks.

o Manages clinical sites and academics institutions, ensures adherence for keeping clinical records, source documents, data entry, manages clinical trial logistics, applications (IRB, local agencies)

- Planning, management and reporting of clinical studies through oversight of cross-functional study activities, identification and resolution of issues, and communication of study timelines/deliverables

- Ensuring implementation and conduct of study(ies) in accordance with ICH-GCP guidelines

o Ensures development, review, finalization and delivery of high quality key study documents in order to meet study timelines.

o Manages CRFs creation, implementation, collaborating closely with data management for the study activities

o Ensures accurate maintenance and archiving of study records

o OverseesTMF

- Management of study budget and timelines

- Management of vendors, including a CRO, to the required standards

Required Knowledge

- Experience & knowledge of clinical project management

- Experience in oversight of external vendors (e.g. CROs, central labs, etc.)

- Understanding of regulatory environment, GCP/ICH

- Experience working in an academic environment is a plus, as well as experience in orphan disease field

Skills and Abilities

- Excellent organisational and communication skills;

- ‘Can-do’ attitude and willingness to be flexible


- BsC in life sciences

Msc/PhD in life sciences is a plus


All employment offers and CV’s are managed through our Human Resources Department and all candidates are presented through this avenue. Therefore, the Human Resources Department at Orchard Therapeutics requests that recruiters are not to contact Orchard Therapeutics employees directly to present candidates. Complying with this request will be a factor in determining future professional relationships with Orchard Therapeutics. Orchard Therapeutics will not accept unsolicited resumes from any source other than directly from candidates for either current or future positions. Submission of unsolicited resumes in advance of an agreement between the Human Resources Department and the recruiter does not create any implied obligation on the part of Orch