Clinical Study, Associate Manager (hybrid)

Highly Competitive
  1. Contract
  2. Project/Study Manager (CSM/CPM)
  3. United Kingdom
London, England
Posting date: 26 Jan 2024
58566

Proclinical are recruiting for a Clinical Study, Associate Manager to join a pharmaceutical organisation. This role is on a contract basis and is located in London with hybrid working available.

Responsibilities:

  • Supervise progress for site activation and oversight visits.
  • Monitor the implementation of the specific clinical study deliverables against planned timelines.
  • Raise any concerns linked to timelines or budget to clinical study lead.
  • Assist on data quality which involves routine evaluation of data metrics and listings, protocol deviations, eligibility violations, dosing deviations and suspected non-compliance by sites.
  • Raise data flow and data quality concerns to clinical study lead.
  • Partake in the development of and supervise execution of recruitment and retention methods.
  • Evaluate site level notified consents and any other patient-facing study start-up resources.
  • Offer routine status reports to shareholders as requested by the clinical study lead.
  • Other duties may be assigned.

Key Skills and Requirements:

  • Educated to a degree level with relevant work experience.

If you are having difficulty in applying or if you have any questions, please contact Matthew Pike at m.pike@proclinical.com.

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

Proclinical Staffing is an equal opportunity employer.

#Clinical

close