Hobson Prior are currently looking for a Senior Clinical Trial Management to join a brilliant biotech organisation on a contract basis located in Uxbridge with hybrid working available. Our client is focused on finding, developing and distributing novel remedies for people who suffer from life-threatening illnesses.

Please note that to be considered for this role you must have the right to work in this location.

Key Responsibilities:

• For this role, you will recognise operational challenged in cooperation with senior team members offering and executing solutions to guarantee studies remain on track.
• Might conduct study CRO oversight tasks, guaranteeing compliance with protocol, regulatory needs, SOPs and oversight plans when needed.
• Offer support in preparing safety, interim and final study dossiers, which involves resolving data discrepancies.
• Uphold internal clinical operations and medical affairs databases and clinical study data and document repositories.
• You might provide aid in the development and evaluation of protocols, notified consents, and case report forms, oversight plans, abstracts, presentations, manuscripts and clinical study reports.
• Assist the CO LP study lead in offering monthly study updates to SMT and any other suitable internal shareholders.
• Execute working procedures to promote high quality, effective and compliance systems for late phase research management.
• Any other assigned duties.

Requirements:

• Educated ideally to a degree level in a pertinent scientific field with pertinent clinical experience within a pharmaceutical, health care organisation or similar.
• An organised individual with the ability to plan and manage own time efficiently.
• Exhibits the core values of working well in a team and responsibility with the capacity to both prioritise competing timelines and deliver brilliant outcomes.
• Learning skills with the ability to be flexible within a fast paced setting.
• Interpersonal, presentation and communication skills both verbally and in writing.
• A high level of customer focus.
• Capable of upholding both internal and external networking and cross-functional cooperation.
• Exhibits a high sense of urgency and commitment to brilliant in the successful implementation of deliverables.
• Capable of prioritising various tasks simultaneously with the ability to complete objectives using well outlines instructions and processes.
• Expertise and comprehension of ICH GCP, FDA and EMEA guidelines and regulations suitable to post-authorisation studies.
• Willing to travel for business needs.

Apply now:

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.