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| Job Field | Discipline | Region | Actions |
| Regulatory And Drug Safety | Director | Berkshire, Hampshire, London - Central, Oxfordshire,... | Details |
| Are you an experienced Pharmacovigilance Manager looking to move into a Director level role? Do you have at least ten years experience in this discipline? If so this is the ideal next step for you, with a large pharmaceutical company based in Hampshire. In this role you will be responsible for both line management as well as developing the role into Europe. Responsibility will be to provide... [Full Details] |
| Salary: 80000 £ |
| Regulatory And Drug Safety | Director | Bedfordshire, Buckinghamshire, Cambridgeshire, Essex,... | Details |
| Senior Manager Clinical QA
Our client a TOP GLOBAL Pharmaceutical company are now looking to recruit again due to expansion; as a large Pharmaceutical company our client provides excellent career progression with exciting and diverse products. An excellent company to take the next step up your career ladder!
Main purpose of the job:
To support the Associate Director, Clinical QA in the... [Full Details] |
| Salary: 45000 £ |
| Regulatory And Drug Safety | Director | Bedfordshire, Buckinghamshire, Cambridgeshire, Essex,... | Details |
| SENIOR PHARMACOVIGILANCE ASSOCIATE (SPVA)
This is an excellent opportunity with a specialised and high innovative small Pharmaceutical company based in the South East. This position will be suitable for a candidates with solid Drug Safety experience seeking to broaden their safety knowledge in both a clinical trial and spontaneous setting and to be part of a progressive department. The... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Director | Any Location (Belgium) | Details |
| We are looking for an Associate Director of Drug Safety for a well known multi national pharmaceutical company. Based in Brussels, this position is integral to the Drug Safety operations.
You will:
•Be a physician with experience within drug safety in the pharmaceutical industry
•Decide on pharmacovigilance strategies
•Write expert and PSUR reports
•Evaluation of benefit/risk ratios
In... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Director | Bedfordshire, Berkshire, Hertfordshire, Oxfordshire,... | Details |
| Superb opportunity with global leading company. Are you experienced in regulatory affairs? Are you confident of your ability to lead a team of regulatory professionals? Do you want to have an international influence? This could be the right role for you. It offers a challenging role as well as industry competitive packages.
You will need?
ï‚· Relevant graduate qualification
ï‚· Proven... [Full Details] |
| Salary: Negotiable (60000 - 80000 £) |
| Regulatory And Drug Safety | Director | Avon, Bedfordshire, Berkshire, Buckinghamshire,... | Details |
| Want to work in a high growth area within the clinical research arena? Interested in working for a global industry-leading organisation? Due to ongoing growth we have immediate Drug Safety Specialist opportunities within an established Pharmacovigilance (PVG) department based in the Cambridge area for a leading Contract Research Organisation (CRO).
Successful candidates will become key... [Full Details] |
| Salary: Negotiable (20000 - 33000 £) |
| Regulatory And Drug Safety | Director | Avon, Bedfordshire, Berkshire, Buckinghamshire,... | Details |
| Want to work in a high growth area within the clinical research arena? Interested in working for a global industry-leading organisation? Due to ongoing growth we have immediate Drug Safety Specialist opportunities within an established Pharmacovigilance (PVG) department based in the North Lanarkshire area for a leading Contract Research Organisation (CRO).
Successful candidates will become... [Full Details] |
| Salary: Negotiable (20000 - 33000 £) |
| Regulatory And Drug Safety | Director | Avon, Bedfordshire, Berkshire, Buckinghamshire,... | Details |
| Interested in working within a global industry leading organisation? Want to work as part of a growing dynamic team? Our client has Safety Administrator opportunities in its offices in Cambridge.
This position, part of the pharmacovigilance team, has responsibility for the tracking of all documents related to the team`s designated projects. Working within the team, the postholder process all... [Full Details] |
| Salary: Negotiable (15000 - 17500 £) |
| Regulatory And Drug Safety | Director | Avon, Bedfordshire, Berkshire, Buckinghamshire,... | Details |
| Interested in working within a global industry leading organisation? Want to work as part of a growing dynamic team? Our client has Safety Administrator opportunities in its offices in North Lanarkshire.
This position, part of the pharmacovigilance team, has responsibility for the tracking of all documents related to the team`s designated projects. Working within the team, the postholder... [Full Details] |
| Salary: Negotiable (15000 - 17500 £) |
| Regulatory And Drug Safety | Director | Avon, Bedfordshire, Berkshire, Buckinghamshire,... | Details |
| Want to work in a high growth area within the clinical research arena? Interested in working for a global industry-leading organisation? Due to ongoing growth we have immediate Drug Safety Specialist positions and Team Manager opportunities within an established Pharmacovigilance (PVG) department for a leading Contract Research Organisation (CRO).
Successful candidates will become key... [Full Details] |
| Salary: Negotiable (30000 - 36000 £) |
| Regulatory And Drug Safety | Director | Bedfordshire, Buckinghamshire, Hertfordshire, Oxfordshire,... | Details |
| This is an outstanding opportunity for an established Regulatory Affairs professional to take a leadership role in a young and exciting company with the opportunity to build an international Regulatory Affairs function in a highly entrepreneurial and evolving environment.
Requirements:
ï‚· Degree in Life Sciences, ideally a qualification in pharmacy or QP
ï‚· Proven track record in a... [Full Details] |
| Salary: Negotiable (65000 - 85000 £) |
| Regulatory And Drug Safety | Director | Buckinghamshire (United Kingdom) | Details |
| The Role and your Responsibilities
DIRECTOR, REGULATORY AFFAIRS for a forward moving CRO
You will be required to: provide effective management, direction and guidance to assigned reporting staff in the successful implementation of their duties.
Effective regulatory affairs consultancy for all projects being undertaken by the division in accordance with company policy, standards and... [Full Details] |
| Salary: Negotiable (65000 - 75000 £) |
| Regulatory And Drug Safety | Director | Any Location (Switzerland) | Details |
| This key executive role offers an outstanding opportunity for an experienced Drug Regulatory Affairs profession to become the Global Director for an international giant in the pharmaceutical world at their office in Switzerland. This will be a highly prestigious position for a company that's well known around the world as a leading name in the discovery, development and marketing of innovative... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Director | Buckinghamshire (United Kingdom) | Details |
| Director of Regulatory Affairs
£Neg, Permanent
South-East
PURPOSE OF THE JOB:
To provide effective Regulatory Affairs consultancy for all projects being undertaken by the Company in accordance with Company Policy, Standards and Procedures. At all times to actively promote the best interests and development of the Company.
JOB FUNCTIONS/RESPONSIBILITIES:
Duties will be variable... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Director | Manchester (United Kingdom) | Details |
| SUMMARY
Our client is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries, who specialise in the strategic development, management and analysis of programmes that support clinical development. Due to continued expansion of the Bioanalytical Department and in order to promote the services of the Bioanalytical facility, a new... [Full Details] |
| Salary: Negotiable (40000 - 60000 £) |
| Regulatory And Drug Safety | Director | New Jersey (United States Of America) | Details |
| This key executive role offers an outstanding opportunity for an experienced Drug Regulatory Affairs profession to become the Global Director for an international giant in the pharmaceutical world at their office in East Hanover, New Jersey. This will be a highly prestigious position for a company that's well known around the world as a leading name in the discovery, development and marketing... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Director | Bedfordshire, Berkshire, Buckinghamshire, Cambridgeshire,... | Details |
| Superb opportunity with global leading company. Are you experienced in regulatory affairs? Are you confident of your ability to lead a team of regulatory professionals? Do you want to have an international influence? This could be the right role for you. It offers a challenging role as well as industry competitive packages.
You will need?
ï‚· Relevant graduate qualification
ï‚· Proven... [Full Details] |
| Salary: Negotiable (Up to 70000 £) |
| Regulatory And Drug Safety | Director | North Carolina (United States Of America) | Details |
| Position Description
Sr. Director Regulatory affairs:
Works independently with only high level direction from senior management to coordinate and facilitate all interactions between the Company and regulatory authorities; develops regulatory strategy and provides regulatory guidance and expertise to various company departments, groups and project teams.
Essential Skills... [Full Details] |
| Salary: Negotiable (125000 - 175000 $) |
| Regulatory And Drug Safety | Director | North Carolina (United States Of America) | Details |
| • Director Regulatory Affairs
OVERVIEW:
This individual will direct all regulatory affairs efforts and requirements for our organzization. Provide professional expertise and strong leadership in the development and implementation of sound regulatory strategies, including meetings with FDA, CMC, clinical trial functions, and issues related to biological product development, submissions, and... [Full Details] |
| Salary: Negotiable (120000 - 170000 $) |
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