Clinical Trials Project Leader
4 weeks ago
Job Title: Clinical Trials Project Leader
Work Location: Uxbridge, London, UK
Work Structure: Monday to Friday, 37.5H/W. 3 days on site required
Contract Duration: 12-months
Pay Rate: £420 - £450
Position Overview:
Join i-Pharm Consulting as a Clinical Trials Project Leader and take on a crucial role in the global execution of Phase I - IV clinical studies across various therapeutic areas. Ensure that clinical studies are conducted in accordance with standard operating procedures (SOPs), company policies, and regulatory guidelines, delivering high-quality data for international product registration and commercialization.
Key Responsibilities:
- Oversee small-scale clinical studies, including Phase I trials.
- Manage the selection of CROs and vendors, ensuring effective communication and deliverables.
- Act as the primary operational contact, supervising site activities.
- Develop logistics and clinical study plans.
- Manage timelines, documentation, and communications throughout the study.
- Participate in project meetings with CROs, vendors, and cross-functional teams.
- Contribute to the development of SOPs and enhance project efficiencies.
- Review regulatory documents to ensure compliance.
- Assist in the preparation of safety, interim, and final study reports.
- Provide training to new or less experienced team members.
Requirements:
We appreciate diverse contributions and seek candidates with the following qualifications:
Minimum Education & Experience:
- PharmD / PhD with 2+ years of relevant clinical experience.
- MA / MS with 3+ years of relevant clinical experience.
- BA / BS / RN with 5+ years of relevant clinical experience.
- Experience managing less complex studies and project teams, including oversight of external vendors.
Knowledge & Skills:
- Quick learner with the ability to adapt to changing circumstances.
- Proficient in managing the complete study lifecycle from initiation to closure.
- Advanced understanding of study management best practices.
- Thorough knowledge of FDA, EMA, and other national regulations, ICH guidelines, and GCP.
- Familiarity with standard medical and scientific terminology.
- Strong communication skills, both clear and concise.
- Team-oriented approach in a highly matrixed environment.
- Able to manage multiple tasks and travel as required.
If you are a motivated and experienced professional ready to make a significant impact in clinical trials, consider joining i-Pharm Consulting's team.
How to Apply:
To apply, please submit your CV detailing your qualifications and experience relevant to this role.
Please note: You must be eligible to work in the UK without restriction or sponsorship to be considered for this role.
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