Clinical Project Manager-Medical Devices
Pharmaceutical Company based in Buckinghamshire
Permanent- Office based
Our client is a leading pharmaceutical company, located in Buckinghamshire. Working across multiple therapy areas, they research and^develop both ethical, consumer health and Medical device products in a range of therapy areas including dermatology, ophthalmology, neurology and other speciality markets.
CSL are privileged to have a longstanding relationship with this client and have made many placements both for permanent and contract openings so can really vouch for them when we say that candidate feedback is extremely positive and this is a great place to work.
Our client is looking to recruit a Clinical Project Manager -Medical Devices (International Role)
You will be responsible for all study management activities associated within Medical Device trials, and will be heavily (hands on) involved in the full lifecycle of your projects working^with the various functions from the monitoring group, study start up, commercial, regulatory across offices globally.
You will ensure that clinical strategies are translated into operational plans and executed in line with clinical development plans. This will include the development and implementation of clinical protocols. In particular you will align operational execution activities with agreed upon project priorities, timings and quality specifications and adhere to all relevant regulations and guidelines including where appropriate: relevant ISO Standards; GCP /ICH; local regulatory requirements; and our clients SOPs and policies. Dependant upon project requirements, the Clinical Project Manager may be required to initiate and monitor clinical sites in the EAME area.
Essential Skills & Qualifications Required
Degree in Life Sciences or related field.
Recent medical devices project management experience is essential
Ideally someone having monitored previously would be highly sought after
Someone used to dealing with Surgeons
Someone familiar with electronic systems
Happy with some travel (25%)
Happy to be in a hands on role as you will carry out some monitoring activities, for example SIVs
Strong experience in^set up
Good site experience
Strong technical expertise
Ability to multi task and priorities
Strong attention to details
Strong communication skills (both internal department and external)
Employer: Pharmaceutical Company
Employment Type: Permanent
Hours: Full time
Location: Office Based in Buckinghamshire with 25% travel
Plan Start Date: Negotiable
Clinical Research, Clinical Operations, Clinical R&D, CRA, CTM, CTA, GCP, Site Manager, Monitor, Manager, Study Manager, EUCTD, ICH GCP, Project Manager, Clinical Study, Clinical Programme, Feasibility, Essential Documents, GCP, SOPs, Compliance, Training,Investigator Meeting, REC, Research Ethics. R&D, Trust, SMO, line Manager, Quality Control, QC
Assigned Consultant: Sue Spice at CSL on 01932 228 928
Please feel free to call for a detailed Job Description or additional information
Applications are reviewed within 24hrs, applicants will only receive feedback if they are suited to the role. The role may^have been remarketed; if you applied for this role previously and were unsuccessful you will not receive a response. We are unable to respond to applicants who are not EU nationals unless they include evidence of right to work in full time employment with their application. Do apply with relevant information on required location or salary/day rate if you are a new