| 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 | QA | 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 |
| QA Manager | Regulatory And Drug Safety | QA | Cambridgeshire, Norfolk, Suffolk... | 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 £) |
| CMC Regulatory Affairs Manager - Global - Switzerland - CHF130+ | Regulatory And Drug Safety | Any Discipline | 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 | Any Discipline | 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 | Any Discipline | 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 | Any Discipline | 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 | Any Discipline | 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 | Any Discipline | 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 Affairs Specialist | Regulatory And Drug Safety | QA | 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 | Any Discipline | 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 | Any Discipline | 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 Affairs Manager | Regulatory And Drug Safety | Any Discipline | 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 £) |
| Senior Regulatory Affairs Specialist - CMC, Global, Midsize Pharma - Contract, SOUTH UK | Regulatory And Drug Safety | Any Discipline | Berkshire, Buckinghamshire, Hampshire,... | 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 |
| Regulatory Affairs Manager | Regulatory And Drug Safety | Any Discipline | Any Location (Denmark) | Details |
| Responsibilities:
- Participation in cross-functional projects on further development of marketed products and expansions to new markets
- Preparation and compilation of quality documentation for new MAAs and for variation applications to the authorities for Marketing Authorisation
- Responsible for submission and the regulatory process in connection with quality variation of MAs and... [Full Details] |
| Salary: Negotiable |
| Head of Regulatory Affairs | Regulatory And Drug Safety | Any Discipline | Any Location (Denmark) | Details |
| In order to be successful in the role of a Head of Regulatory Affairs – Established Products Unit, you will be an experienced Regulatory professional with extensive knowledge of Global Regulatory Affairs and an entrepreneurial mind set. You will be a hard-working and experienced team leader, who has the drive to build and develop a new department.
As a Head of Regulatory Affairs you will... [Full Details] |
| Salary: Negotiable |
| Global CMC Regulatory Affairs Manager - Switzerland | Regulatory And Drug Safety | Any Discipline | Any Location (Switzerland) | Details |
| As a Regulatory Affair Manager you will be responsible for the management of all the CMC regulatory activities in the EMEA/US/International markets that apply to medicinal products, medical devices, cosmetics and food supplements in my client's vast product portfolio.
Responsibilities include, but are not limited to:
• Ensure the promotional materials are in compliance with the... [Full Details] |
| Salary: Negotiable (130000 - 140000 £) |
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