Project Manager (Clinical Research) –£35,000-£50,000 + Benefits– Home based, with travel to clinical sites as required.
The Role
Are you a clinical research professional looking to advance your career? Do you have the expertise to manage clinical projects efficiently while ensuring compliance with regulatory standards? If so, we have an exciting opportunity for you.
We are a full-service UK clinical trial site, providing virtual and decentralised clinical trial services, looking to appoint an experienced Project Manager to our growing team.
In this role, you will be crucial in driving clinical projects forward and ensuring that we meet our clients' needs. Reporting directly to the Clinical Operations Manager, you will also have the potential to advance into more senior roles within our organisation.
If you are an experienced clinical research manager with a commitment to excellence, apply today to be part of a pioneering organisation that brings clinical trials to patients and accelerates market access for new products.
Key Responsibilities:
- Project Planning and Execution: Develop project plans outlining timelines, milestones, resources, and deliverables for clinical trials. Ensure that all project activities are completed on time and within budget.
- Team Coordination: Collaborate with cross-functional teams, including clinical staff, data management, regulatory affairs, and sponsors, to ensure smooth and effective trial operations.
- Communication: Serve as the primary point of contact between the clinical trial site and sponsors, providing regular updates on project status, timelines, and any potential issues.
- Risk Management: Identify potential risks and challenges in the trial process and develop mitigation strategies to address them proactively.
- Regulatory Compliance: Ensure that all trial activities are conducted in compliance with applicable regulatory guidelines, including Good Clinical Practice (GCP), and local regulations.
- Budget Management: With guidance and input from the Clinical Operations Manager, oversee the financial aspects of the trial, including budget development, tracking expenses, and ensuring that the project stays within financial constraints.
- Documentation and Reporting: Maintain accurate and up-to-date documentation for all trial activities, including project plans, meeting minutes, and progress reports.
- Quality Control: Monitor the quality of the trial's conduct and data collection processes, ensuring adherence to protocols and SOPs.
- Training and Development: Provide guidance and training to clinical staff as needed, ensuring they are well-prepared to execute the trial according to protocol.
The Company
VCTC is a UK based patient centric clinical trial site that eliminates the burden of participation and facilitates the rapid recruitment of patients. Our pioneering processes take clinical trials to our patients, providing access to all, generating diversity and quality data through a compassionate, expedited virtual clinical trial process.
At our core we enhance the clinical trial experience for participants and sponsors leading to expedited timelines, reduced cost and ultimately bringing products to market quicker.
This is, and always will be, a core part of VCTC.
VCTC is an equal-opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
The Benefits
- Pension.
- 35 hour working week
- Private medical insurance.
- Company bonus scheme.
The Person
- Advanced degree or PMP certification, or a commensurate amount of experience in a clinical trial or healthcare setting.
- Strong understanding of clinical trial processes, regulations, and best practices.
- Excellent organisational, problem-solving, and multitasking skills.
- Strong communication and interpersonal skills, with the ability to work effectively with diverse teams.
- Proficiency in project management software and tools.
- Ability to work independently and manage multiple projects simultaneously.