Hobson Prior are looking for a Senior Clinical Operations Manager to join a leading pharmaceutical organisation in London to be responsible for overseeing and managing clinical trials on behalf of the organisation.

Job Responsibilities:

• Represent as the main point of contact for all study operational management related communications with Service Providers /Contractors and the organisations Development HQ.
• accountable for setting up, implementation and reporting of clinical trials working with the project team and external Service Providers /Contractors.
• Managing SPs/Contractors and overseeing their performances and quality of work to ensure they meet the project plan, contracts and any study specific requirements.
• Developing and maintaining study documents with internal and external project teams.
• Organizing and chairing the monthly project meetings.
• Organizing study meetings / training as required.
• As an overseeing role, supervising, mentoring and assisting COMs, when required, to ensure adherence to agreed project plan, budget, and quality specifications for individual clinical trials.
• Taking a leading role and contributing to development and maintenance of company policies, SOPs and OPUK documents.
• Ensuring learning and knowledge transfer during and at the completion of the clinical trials.

Key Skills:

• Excellent computer skills in Word, Excel, PowerPoint, email and Internet.
• Flexibility and the ability to handle multiple tasks to meet deadlines while delivering high quality work in a dynamic environment.
• Able to interact effectively at all levels within the organisation, as well as with external partners and clients.
• Strong written and spoken English.
• Excellent communication skills (verbal and written).
• Excellent organisational, presentation and time management skills.
• Must be meticulous and methodical, with the ability to review both data and procedures in detail and the ability to see and communicate the greater overall picture.

Requirements:

• Minimum BSc in the life sciences, nursing degree, or equivalent combination of education and experience.
• Significant demonstrable clinical research experience gained within a contract research organisation, pharmaceutical, or Biotechnology Company.
• Proven experience of technical and/or project management in conducting multi-national and/or single site early phase clinical trials in a pharmaceutical company or CRO.
• In-depth knowledge of regulatory requirements, clinical development, and clinical monitoring procedures.
• Demonstrable experience of leading project/study teams.
• Ability to oversee and manage CROs throughout the entire clinical operations life cycle of a study.
• Demonstrated proficiency with ICH/GCP guidelines.
• Experience working in and motivating a team under time and resource pressures to meet objectives.

Apply now:

If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back 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.