Similar posts
Contract Clinical Trial Management Assoc
- Contract
- Project/Study Manager (CSM/CPM)
- United Kingdom
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.
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
Related jobs
Highly Competitive
Uxbridge, England
We are on the hunt for bold, innovative thinkers who are ready to help push the boundaries of science and make a tangible difference in the world.
US$70 - US$90 per hour
Cambridge, USA
Are you ready to lead cutting-edge IRT projects that accelerate clinical breakthroughs in biotech?
Highly Competitive
Cambridge, USA
Be the driving force behind clinical operations and help shape the future of pharma innovation.
Highly Competitive
Collegeville, USA
Are you ready to turn precision into progress and play a key role in shaping the future of pharmaceutical innovation?