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Regulatory Affairs - Director of Regulatory Affairs Jobs - Buckinghamshire

Regulatory Affairs - Director of Regulatory Affairs Jobs - Buckinghamshire (Job Ref: WR/JOBS/24682-11109)

Job Description :

Flame Pharma Regulatory Affairs - Director of Regulatory Affairs Job - Buckinghamshire:

Job Summary

An excellent opportunity has arisen for an experienced Director of Regulatory Affairs to join one of the world’s leading Contract Research Organisations.

Our client, Global experts in Clinical Pharmacology, Regulatory Affairs, Pharmacokinetics, Pharmacometrics, Biopharmaceutics, and Bioanalytical, are looking to offer the ideal candidate full support and extensive, consistent and continuous training to reach their goal.

They are looking for a professional and enthusiastic Director of Regulatory Affairs to join their dedicated team based in Buckinghamshire.

Job Title

Director of Regulatory Affairs

Background

As Director of Regulatory Affairs you will provide effective management, direction and guidance to assigned reporting staff in the successful implementation of their duties.

Key Responsibilities

· To provide effective regulatory affairs consultancy for all projects being undertaken by the division in accordance with company policy, standards and procedures.

· To provide and co-ordinate appropriate resourcing to ensure effective support of consulting projects.

· To develop and promote effective Regulatory Affairs services in Italy by developing local relationships and collaborating with BD in securing new business for the Division.

· To provide effective senior management support to the vice-president in the attainment of the division’s business and financial goals and to act as a deputy/designee to the vice president as and when required.

· At all times to actively promote the best interests and development of the Company.

· To provide project management or oversee assigned project managers in their duties relating to regulatory projects from Italian clients or relating to Italy.

· To provide effective input and support for all relevant projects where regulatory consulting is an area of focus.

· As a member of the Senior Management Team, to proactively contribute to the successful performance of that team and to carry out agreed duties and assignments in a timely manner.

· To provide effective management and mentoring of reporting staff including all necessary training to maintain and improve their job performance and knowledge.

· To provide timely input where required into the preparation of project proposals.

· To input and agree the assignment of reporting staff to appropriate project teams.

· To provide effective input and support into BD strategies particularly in relation to Italy and to assist with planning/implementation of local marketing strategies /objectives in that country.

· To develop and maintain strong and positive client and staff relationships.

· To identify opportunities for work flow and/or process improvements and initiate the processes for creation of plans for improvement(s) and implementation of plans.

· To keep the Vice President informed of the progress of relevant activities and projects at all times.

· When acting as a project manager,to carry out the established range of duties relating to this role including effective management of budgetary matters.

· When acting as a project member,to keep the project manager informed of the progress of relevant activities.

· To perform any other reasonably related duties as may be determined from time to time.

· Responsible for overall administration and job performance. · Responsible for specific projects where appropriate.

Qualifications and Experience

· Degree or equivalent in an appropriate discipline, for example, Pharmacy, Pharmacology, Chemistry, Biological Sciences.

· Extensive experience in international regulatory affairs in the pharmaceutical industry with further experience in senior management positions.

Benefits

With this position comes an attractive salary that you would associate with a world leader.

Key Words

Director of Regulatory Affairs, Clinical Research, Study Management, Research, Pharmaceutical, CRO, Clinical Trials, Career, Medical, Clinical, Clinical Management, Job, Recruitment, Buckinghamshire.

This position will be based in Buckinghamshire.

For further information about this role, please contact Flame Pharma.