We are a high-achieving research-led clinic operating from a modern, purpose-built premises working with a multidisciplinary team of highly skilled specialists ranging from Aesthetic Practitioners, Sonographers and Consultant Surgeons..
Hours: 40 hours per week – Clinic Based with option for some remote working.
Salary: £28,000 to £30,000 per year (Depending on experience)
Responsibilities:
The benefits of joining our team:
Salary: £28,000.00-£30,000.00 per year
Benefits:
Expected start date: 30/06/2023
Hours: 40 hours per week – Clinic Based with option for some remote working.
Salary: £28,000 to £30,000 per year (Depending on experience)
Responsibilities:
- Manage and provide accountability for day-to-day operations of the project, as defined and according to ICH/GCP/Medical device and all other applicable laws, rules, and regulations.
- Serve as primary contact for operational project-specific issues and study deliverables.
- Maintain in depth knowledge of protocol, therapeutic area, and indication.
- Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided.
- Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable
- Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables.
- Coordinates cross functional teams and acts as the main point of contact with for a country with the protocol manager and other global study team members.
- Local vendor assessment and set up during study start-up (as applicable)
- Investigator Meeting participation and preparation
- Ensures data entered in Clinical Trial Managements Systems is current and complete and access to eDC and vendor systems is available for internal and clinical trial site personnel.
- Validation of study related materials (i.e. protocol, ICF, patient material)
- Responsible for preparing country specific documents (e.g. global country specific amendment)
- Coordination of database locks and query follow up. Ensures timelines are met.
- Management of clinical trial site relationships
- May conduct Pre-Study Evaluation Visits (PSEVs) and Site Initiation Visits (SIVs)
- May perform site closure activities, including post-close out.
- May act as point of contact for Sites.
- May support preparing submissions to and obtaining approval from local Health Authorities, Ethics Committees and other relevant instances.
- Support and organise summer research program at The Whiteley Clinic. (6 weeks program)
- Set up and run research projects.
- Bachelor’s degree in a health or life science-related field; Advanced degree in a health or life science-related field preferred.
- Experience in Phases 1-4; Phases 2-3 preferred.
- Minimum of 2 years of Clinical Trial Management experience.
- 3+ years of Project Manager/Clinical Trial Manager experience.
- Good verbal and written communication skills (both in English and local language).
- Good working knowledge of following Software: Microsoft Suite, Clinical Trial Management Systems (CTMS), Electronic Data Capture Systems (eDC), Electronic Trial Master File (eTMF).
- Management of overall project timeline. Strong leadership skills.
The benefits of joining our team:
- Joining a team passionate on developing individuals to maximise their potential.
- 25 days + bank holidays allowance
- An extra day off to celebrate your birthday.
- Excellent private pension scheme
- Private Health Care
- Joining a world renowned Clinic.
- Discounts at our Aesthetics Clinic
Salary: £28,000.00-£30,000.00 per year
Benefits:
- Company events
- Company pension
- Cycle to work scheme
- Employee discount
- Free parking
- On-site parking
- Private medical insurance
- 8 hour shift
- Monday to Friday
- Performance bonus
- Guildford: reliably commute or plan to relocate before starting work (required)
- Bachelor's (preferred)
- clinical trial management: 2 years (preferred)
Expected start date: 30/06/2023
