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| Job Field | Discipline | Region | Actions |
| Regulatory And Drug Safety | Clinical Project Manager, Drug Safety | Hertfordshire (United Kingdom) | Details |
| Our client based in north Hertfordshire is looking for a Team Leader, Safety Surveillance and Risk Management. The ideal candidate should have a minimum of at least 4-5 years Pharmacovigilance. This role is directly line managing a team of 3 people.
1) Act as a Safety Surveillance and Risk Management - Team Leader with 3 direct reports.
2) Periodic Safety Update Reports (PSUR) –... [Full Details] |
| Salary: Negotiable (40000 - 45000 £) |
| Regulatory And Drug Safety | Clinical Project Manager, Drug Safety | Hertfordshire (United Kingdom) | Details |
| Our client based in north Hertfordshire is looking for a Team Leader, Safety Surveillance and Risk Management. The ideal candidate should have a minimum of at least 4-5 years Pharmacovigilance. This role is directly line managing a team of 3 people.
1) Act as a Safety Surveillance and Risk Management - Team Leader with 3 direct reports.
2) Periodic Safety Update Reports (PSUR) –... [Full Details] |
| Salary: Negotiable (40000 - 45000 £) |
| Regulatory And Drug Safety | Clinical Project Manager, QA, Drug... | Any Location (France, Germany, United Kingdom) | Details |
| JOB ROLE:
The Senior Quality Assurance Auditor is responsible for the Quality Assurance aspects of clinical trials, ensuring trials conform to ICH-GCP, other applicable regulations and the relevant Standard Operating Procedures (SOPs). The Senior Quality Assurance Auditor is independent of the Clinical Research Team.
PRINCIPAL RESPONSIBILITIES include:
• Supervision of QA Auditors... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Regulatory Affairs | London (United Kingdom) | Details |
| My client is a medical communications agency who offers the full range of medical communications, including regulatory writing services to their clients. As an international agency with the backing of a global group, they have built their reputation on excellence, creativity, and transparency.
Due to phenomenal growth and business won, they require an experienced regulatory medical writer to... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Cambridgeshire, Norfolk, Suffolk (United Kingdom) | Details |
| Experienced Quality Assurance (QA) Manager required by niche CRO. The successful candidate will develop and improve Quality Systems, manage QA activities and collate and report quality metrics to the management team.
A QA Manager is required by our client, one of the largest niche clinical data management and statistics CROs in Europe. They are seeking an individual who is passionate about... [Full Details] |
| Salary: Negotiable (35000 - 37000 £) |
| Regulatory And Drug Safety | Regulatory Affairs | Berkshire, Buckinghamshire (United Kingdom) | Details |
| Regulatory Affairs Manager required by pharma company to support regulatory strategy and operational implementation in the European region. European regulatory experience essential.
Our client is seeking a Regulatory Affairs Manager. Candidates must have good solid experience of lifecycle management with some experience of obtaining new licences. This is a regional rather than a local role so... [Full Details] |
| Salary: Negotiable (Up to 50000 £) |
| Regulatory And Drug Safety | Regulatory Affairs | Berkshire, Buckinghamshire, Hampshire, London, Surrey,... | Details |
| Regulatory Affairs Executive
12 Month Contract
Excellent Rate
Berkshire
An exciting opportunity has arisen with a global Pharmaceutical company who have a leading portfolio of medicines and healthcare products.
Key Responsibilities:
*To manage lifecycle submissions and provide Regulatory Strategy for all registration activities within the countries under responsibility
*To apply... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Drug Safety, Pharmacovigilance,... | Bedfordshire, Buckinghamshire, Hertfordshire, London,... | Details |
| Job Summary:
Regulatory Affairs role within mid sized Pharma Company in Hertfordshire. Summary - Maintain marketing authorisations for both the UK and Ireland to meet regulatory requirements. Provide a medical information service and monitoring/reporting of Pharmacovigilance cases to meet regulatory and legislative requirements. Ensure compliance to company policies and procedures with respect... [Full Details] |
| Salary: Negotiable (25000 - 30000 £) |
| Regulatory And Drug Safety | Clinical Project Manager, Regulatory... | Any Location (Switzerland) | Details |
| CMC Regulatory Affairs Manager – Switzerland – CHF130K+
My client, a large global pharmaceutical company, is currently undergoing an extensive business expansion. Therefore they are looking for top Regulatory industry professionals to join their team. For a confidential discussion call Nikolay on +44 (0) 207 255 6665 or send an e-mail to Nikolay.dimitrov@secpharma.com
On this... [Full Details] |
| Salary: Negotiable (130000 - 140000 £) |
| Regulatory And Drug Safety | Clinical Project Manager, Regulatory... | Any Location (Germany) | Details |
| Regulatory Affairs Manager – Mature Brands - Germany -
To find out more about the company call Nikolay on +44 (0)207 255 6665 or e-mail Nikolay.dimitrov@secpharma.com
My client - an international medium-sized pharmaceutical company is looking to recruit a Regulatory Affairs Manager to join their team based in the global headquarters in Germany. You will be responsible for all activities... [Full Details] |
| Salary: Negotiable (70000 - 90000 £) |
| Regulatory And Drug Safety | Clinical Project Manager, Regulatory... | Any Location (Germany) | Details |
| My client, a generic international company is looking for a Head of Regulatory Affairs in their site in Southern Germany. For a confidential discussion, please call Nikolay on +44 (0) 207 255 6665 or e-mail your CV to Nikolay.dimitrov@secpharma.com
As a Head of Regulatory Affairs you will be responsible for the compilation of the technical documentation and related documents for global... [Full Details] |
| Salary: Negotiable (80000 - 100000 £) |
| Regulatory And Drug Safety | Clinical Project Manager, Drug Safety | Any Location (Switzerland) | Details |
| 1. Develops with PVLs/BSLs AE assessment and coding conventions for oncology pro-jects/products and prepares event specific questionnaires
2. Assists with ad hoc literature searches through initiation of process and screening reports and preparation of summary to be reviewed by PVL or BSL.
3. Facilitates reconciliation with clinical trial data in close collaboration with PVO and ensures... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Clinical Project Manager, Regulatory... | Cheshire (United Kingdom) | Details |
| We are currently recruiting for a Regulatory Affairs Project Manager to join a leading pharmaceutical company, on an initial 9 month contract. Based in Cheshire, this role is full time and office based.
As a Regulatory Affairs Project Manager your responsibilities will include project managing successful regulatory approvals, the maintenance of product licenses and regulatory compliance... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Clinical Project Manager, Regulatory... | Any Location (United Kingdom) | Details |
| Associate Director, Regulatory Affairs / Study Start Up, South East England
Associate Director, Regulatory & Study Start Up, required to join a global Clinical Research Organisation. You will have line management responsibilities for a Regulatory team and be responsible for the development of regulatory business. Permanent opportunity based in South East England.
JOB... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Clinical Project Manager, Regulatory... | Berkshire (United Kingdom) | Details |
| Regulatory Affairs Manager– Maidenhead, UK / home based – 60K+
Regulatory Affairs Manager required for an exciting opportunity with a highly reputable Clinical Research Organisation. You will be responsible for leading the regulatory functions within a group setting. Office based in Maidenhead but part home based working happily considered for right candidates.
JOB TITLE... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Regulatory Affairs | Any Location (Belgium, Germany, Italy, Poland, United... | Details |
| Medpace, a leading therapeutically-focused CRO is growing in Europe. We are looking for key managers to join our Clinical Operations Team to manage European-wide, clinical trial application submissions and overall start up processes. The position is office based to enable support of office based staff. The Regulatory Submissions Manager serves as an important leader on the project team and a... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Regulatory Affairs | Any Location (Germany, Spain) | Details |
| Join one of the industry’s most experienced and specialized clinical trial management teams. Medpace is a global, full-service clinical research organization with expertise and therapeutic specialization in cardiovascular, endocrine/metabolic, and oncology research. We have steadily expanded operations in nearly forty countries. Headquarters are located in Cincinnati, Ohio, with operations in... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Drug Safety, Pharmacovigilance | Any Location (Luxembourg) | Details |
| Our client, a leading European pharmaceutical company is looking to recruit a:
Junior Pharmacovigilance Officer (m/f)
for their Head Office in Luxembourg.
Major responsibilities:
Agreements / Archive.
- Develop and maintain an effective Pharmacovigilance archiving process and ensure that all data is kept in an inspection and audit ready state at all times
- Assist in the drafting and... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA, Regulatory Affairs | Any Location (United Kingdom) | Details |
| The Specialist will be responsible for providing a service to improve compliance of the Technical Files and Design Dossiers required for CE Marking product. The role will involve ensuring that relevant data is identified, supplied and incorporated into the Technical Documentation. The Specialist will maintain up to date knowledge of the related procedures and assist with any improvements... [Full Details] |
| Salary: Negotiable (23 - 25 £) |
| Regulatory And Drug Safety | Drug Safety, Pharmacovigilance | Any Location (Germany) | Details |
| Working within a global Pharmacovigilance team for a large Pharmaceutical company, you will be responsible for:-
Sue of adverse event reports from clinical studies and reports from the licensees of operational units in the European Region
Coding of adverse event reports with medical dictionaries MedDRA, WHO Drug Dictionary
Active tracking of discrepancies in the context of Adverse event... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Clinical Project Manager, Director | Any Location (Czech Republic) | Details |
| INTERNATIONAL ROLE:
My client a multinational generics company and a group of powerful pharma cluster, who has carved out an industry leading reputation in delivering high quality generic products to countries in Europe and Central Asia, currently has a high profile opening for an International Compliance Officer/ Manager ? Internal Audits. This position also welcomes and is open to for... [Full Details] |
| Salary: Negotiable (50000 - 57000 £) |
| Regulatory And Drug Safety | Clinical Project Manager, Regulatory... | Any Location (Belgium) | Details |
| RA Coordinator - BeNeLux
My client, a Major Global Pharmaceutical company is currently looking for a Regulatory Affairs Coordinator to join their team on a 12 months contract basis in one of their offices in Belgium. Under supervision of the Regulatory Affairs Country Lead, you will be responsible for providing regulatory administrative support and coordination for the department with... [Full Details] |
| Salary: Negotiable (30 - 80 £) |
| Regulatory And Drug Safety | Clinical Project Manager, Regulatory... | Any Location (Germany) | Details |
| My client, a generic international company is looking for a Head of Regulatory Affairs in their site in Southern Germany. As a Head of Regulatory Affairs you will be responsible for the compilation of the technical documentation and related documents for global submissions.
Your responsibilities:
- Management and guidance of the regulatory department within the finished dosage form... [Full Details] |
| Salary: Negotiable (80000 - 100000 £) |
| Regulatory And Drug Safety | Clinical Project Manager, Regulatory... | Any Location (Germany) | Details |
| My client is a global medium-sized pharmaceutical company with its head office in Germany. They are looking for Regulatory Affairs Managers to join their Drug Development and Life Cycle Management teams. Depending on the team you join you will be responsible for the strategic development activities related to either drug development or life cycle management of global products.... [Full Details] |
| Salary: Negotiable (70000 - 90000 £) |
| Regulatory And Drug Safety | Regulatory Affairs | Berkshire, Buckinghamshire, Hampshire, London,... | Details |
| Regulatory Affairs, CMC, pharmaceutical, contract, day rate – Exciting new 11month contract position, paying a competitive day rate, has arisen for a Senior Regulatory Specialist (CMC) for this global, award-winning Top 20 Pharmaceutical. Working from their offices in Berkshire/Hampshire region the role has global scope in Regulatory, CMC activities for crucial clinical trials.
Perfect for... [Full Details] |
| Salary: Negotiable |
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