| Job Title | Job Field | Discipline | Region | Actions |
| Team Leader, Safety Surveillance and Risk Management | Regulatory And Drug Safety | Any Discipline | 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 £) |
| Team Leader, Safety Surveillnace & Risk Management | Regulatory And Drug Safety | Any Discipline | 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 £) |
| Senior Clinical QA GCP Auditor - Europe | Regulatory And Drug Safety | Any Discipline | Any Location (France, Germany, United... | 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 Medical Writer – South East England | 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 Affairs Manager | Regulatory And Drug Safety | Regulatory Affairs | Berkshire, Buckinghamshire (United... | 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 Affairs Executive | Regulatory And Drug Safety | Regulatory Affairs | Berkshire, Buckinghamshire, Hampshire,... | 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 Affairs & Medical Information Officer, Post Marketing – Watford, Hertfordshire | Regulatory And Drug Safety | Regulatory Affairs | Bedfordshire, Buckinghamshire,... | 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 £) |
| CMC Regulatory Affairs Manager - Global - Switzerland - CHF130+ | Regulatory And Drug Safety | Regulatory Affairs | 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 £) |
| Global Regulatory Affairs Manager - Branded Products - Germany | Regulatory And Drug Safety | Regulatory Affairs | 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 £) |
| Head of Regulatory Affairs - Germany - EUR 100k | Regulatory And Drug Safety | Regulatory Affairs | 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 £) |
| Pharmacovigilance Scientist (Switzerland) | Regulatory And Drug Safety | Any Discipline | 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 |
| Jr. Regulatory Project Mgr - International Markets | Regulatory And Drug Safety | Regulatory Affairs | 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 |
| Associate Director,Regulatory Affairs/Study Start Up,SE England | Regulatory And Drug Safety | Regulatory Affairs | 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 Affairs Manager– Maidenhead, UK / home based – 60K+ | Regulatory And Drug Safety | Regulatory Affairs | 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 Submissions Manager | Regulatory And Drug Safety | Regulatory Affairs | Any Location (Belgium, Germany, Italy,... | 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 Submissions Coordinator | 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 Affairs Specialist | Regulatory And Drug Safety | 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 £) |
| Internal Auditor / Compliance advisor - PRAGUE | Regulatory And Drug Safety | Any Discipline | 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 Affairs Coordinator | Regulatory And Drug Safety | Regulatory Affairs | 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 £) |
| Head of Regulatory Development Centre | Regulatory And Drug Safety | Regulatory Affairs | 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 £) |
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