Associate Director, Late Phase Clinical Development & Operations, Europe. - Permanent role
Surrey based Pharmaceutical company, growing team, with diverse therapy area responsibilities.
I'm handling a senior role in European Medical Affairs which is located west of London , in Surrey. The role is working for a leading pharmaceutical company and involves strategic life cycle management and product support within Europe. I am looking for a candidate with a proven track record in medico marketing, Phase IV study management brand liaison, trial design and protocol construction and of course delivery of major studies in Europe.
The role has an EU focus and requires some travel for KoL, vendor and product outreach initiatives. You^will not only want the responsibility for delivering a product which meets commercial needs but also be comfortable with study leadership across functions outside clinical operations and within vendor and affiliate led models.
Essential Skills &^Qualifications Required
B Sc a minimum, and ideally a further life sciences degree
Extensive clinical trial experience in CRO, Pharmaceutical or Biotech company, much of which should have been at project manager level
Clinical trial monitoring experience and site and CRO management experience
Thorough knowledge of GCP, IRB/EC process, and other applicable regulatory processes
Ability to work independently on assignments
Ability to identify and resolve project issues
Demonstrate strong organisational skills, including ability to prioritise
Strong clinical study management skills (including project and financial management)
Excellent presentation, organisation, negotiation and management skills
Software Competence Required
- Intermediate MS WORD, - Intermediate EXCEL, - Intermediate Powerpoint
Employer: Pharmaceutical Company
Employment Type: Permanent
Hours: Full time
Location: Office Based near M25 / M3 interchange
Clinical Research,^Clinical Operations, Clinical R&D, CTM, , CRM, GCP, Study Manager, EUCTD, ICH GCP, Project Manager, Clinical Study, Clinical Programme, Feasibility , medical affairs, transplant, urology
Essential Documents, GCP, SOPs, Investigator Meeting, REC, Research Ethics. R&D,
Assigned Consultant:Avril Horn at CSL on 01932 234686
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 candidate.