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Clinical Logistics Senior Specialist
- Contract
- Clinical Evaluation
- United Kingdom
This vacancy has now expired. Please see similar roles below...
Proclinical is seeking a Clinical Logistics Specialist who will be responsible for managing the logistics of investigating products, ensuring provenance and traceability. This role involves collaboration with various stakeholders, including clinical trial personnel, Clinical Operations, Data Management, Clinical Development, Medical Affairs, Regulatory Affairs, Technical Operations, Manufacturing, MSAT, and Quality.
Please note that to be considered for this role you must have the right to work in this location.
Responsibilities:
- Manage clinical logistics and participate in cross-functional project teams.
- Act as the primary liaison for the screening and enrollment of clinical trial participants.
- Coordinate all aspects of study participant sample collection and "cell journey".
- Communicate study requirements and ensure adherence to the cell journey process.
- Assist in refining and improving the cell journey process.
- Prepare metrics and updates for management and identify potential study issues/risks.
- Work with contract research organizations to communicate detailed timelines.
- Lead internal team meetings and provide training at investigator meetings.
- Participate in the development, review, and implementation of departmental SOPs and processes.
- Create and manage clinical logistics programs.
- Support cross-functional projects and travel as required.
Key Skills and Requirements:
- Relevant clinical or logistics experience.
- Knowledge and/or experience with Clinical Trials, Cell Therapy is a plus.
- Ability to work with multiple database and electronic systems.
- Strong analytical and problem-solving skills with attention to detail.
- Excellent organizational skills with the ability to multi-task and prioritize.
- Excellent interpersonal, verbal and written communication skills.
- Comfortable in a fast-paced environment with minimal direction.
- Knowledge of FDA and ICH requirements as they pertain to clinical trials.
- Knowledge of domestic and international logistics/transport of biologic material.
- Ability to manage processes and teams, author documents, and present at study meetings.
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.
If you are having difficulty in applying or if you have any questions, please contact Joshua Bye at j.bye@proclinical.com.
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.
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