Contract Clinical Trial Management Assoc

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.

Responsibilities:

• 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.

#Clinical