Contract Clinical Trial Management Assoc

Highly Competitive
  1. Contract
  2. Project/Study Manager (CSM/CPM)
  3. United Kingdom
London, England
Posting date: 28 Nov 2023

This vacancy has now expired. Please see similar roles below...

Proclinical are recruiting for a Contract Clinical Trial Management Assoc to join a pharmaceutical organisation. This role is on a contract basis and is located in the UK.


  • Guarantee all budget or drug supply modifications are suitably approved, documented and tracked.
  • Execute working procedures to promote high quality, effective, and compliant systems for late phase research management.
  • Preserve internal clinical operations and medical affairs databases, tracking systems and clinical study data and document repositories.
  • You will serve as the main point of contact for external investigators and internal shareholders.
  • Review scientific submissions or protocols to recognise logistical, regulatory and safety elements and implications.
  • Recognise operational challenges and cooperate with senior team members, offering and executing solutions to guarantee studies remain on track.
  • Assist the study drug planning and shipping actions with the company's clinical supply chain management teams.
  • Offer monthly study updated to the suitable internal shareholders.
  • Other duties may be assigned to this role.

Key Skills and Requirements:

  • Educated to a degree level in a pertinent scientific field with demonstrable clinical work experience in a pharmaceutical or healthcare organisation.
  • An organised individual with the ability to plan and manage own time efficiently.
  • Administrative capabilities.
  • Exhibits the core values of teamwork and responsibility with the capacity to prioritise competing timelines and deliver brilliant outcomes.
  • Capable of learning new skills with a flexible mindset to uphold a fast pace.
  • Interpersonal, presentation and communication skills both verbally and in writing.
  • Customer focus.
  • Works well with others and able to maintain said relationships.
  • A sense of urgency and commitment to brilliant within successfully implementing deliverables.
  • Able to prioritise various tasks simultaneously while completing objectives.
  • Comprehension of ICH GCP, FDA and EMEA guidelines.
  • Computer literacy.
  • Knowledge of routine medical/scientific vocabulary.
  • Capable of partaking in divisional and interdivisional methodical initiative under general supervision.
  • Able to participate in SOP development when required.

If you are having difficulty in applying or if you have any questions, please contact Matthew Pike on +44 207 4400 639.

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.