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| Job Field | Discipline | Region | Actions |
| Regulatory And Drug Safety | Regulatory Affairs | Bedfordshire, Buckinghamshire, Cambridgeshire,... | Details |
| Our client is a leading Biopharma with a global presence. They are currently looking for an experienced Regulatory Operations professional to join their team. You will receive a very competitive salary and benefits package and an opportunity to develop into the senior manager levels as the company continues to expand.
Requirements:
Degree educated, preferably in a life sciences... [Full Details] |
| Salary: Negotiable (35000 - 40000 £) |
| Regulatory And Drug Safety | Pharmacovigilance | Bedfordshire, Berkshire, Buckinghamshire, Cambridgeshire,... | Details |
| An exciting opportunity has arisen in the safety surveillance department of this leading Biopharmaceutical Company. The position requires someone who is not only very experienced in pharmacovigilance but also someone who is able to manage both projects and junior colleagues. In return you will receive an industry leading compensation package as well as having significant future... [Full Details] |
| Salary: Negotiable (5000 - 60000 £) |
| Regulatory And Drug Safety | Drug Safety | North Carolina (United States Of America) | Details |
| Product Safety Specialist
RTP, NC
Requirements
The Product Safety Specialist is responsible for coordinating and performing adverse event data entry, review of entered cases, follow-up with reporter and/or associated HCP, tracking of reports, and reporting activities. He/she must maintain knowledge and understanding of PPD and client-provided SOPs and current FDA regulations. He/she... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Clinical Project Manager, Drug Safety,... | North Carolina (United States Of America) | Details |
| This is an excellent opportunity for a clinical research professional with substantial Pharmacovigilance / Drug Safety experience to join a unique, full service CRO that specializes only in studies using EDC. They manage Phase I-IV clinical trials online for leading biopharmaceutical and medical device organisations, combining advanced technology with expert clinical knowledge and experience in... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA, Regulatory Affairs | Hampshire (United Kingdom) | Details |
| Our client is a leader is development of surgical equipment as well as playing a central role in the development of products that are used in various sugery operations. They are looking for a Regulatory Affairs and Quality Assurance Coordinator with experience working with the FDA, MHRA, Technical Dossiers, ISO13485 and ISO9001.
This position will require you to work to ensure compliance with... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | London - Central (United Kingdom) | Details |
| Our client is a Contract Research Organisation specialising in Phase 1 of Clinical Trials based in the Greater London area offering excellent facilities and an attractive client base. As a QA GCP Manager you will be at the forefront of leading the auditing team as well as ensuring a good standard of service is offered to the clients in the bid for further business development.
As the QA... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | London - Central (United Kingdom) | Details |
| As the QA Manager you will be responsible for planning, preparing and reporting on clinical audits to ensure trials conform to applicable regulations, GMP guidelines, ICH-GCP and the relevant Standard Operating Procedures (SOPs). This includes responsibilities for arranging and conducting procedural audits on individual studies and/or specific areas of Unit's operations, as determined by... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | London - Central (United Kingdom) | Details |
| As the QA Manager you will be responsible for planning, preparing and reporting on clinical audits to ensure trials conform to applicable regulations, GMP guidelines, ICH-GCP and the relevant Standard Operating Procedures (SOPs). This includes responsibilities for arranging and conducting procedural audits on individual studies and/or specific areas of Unit's operations, as determined by... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Surrey, London - South (United Kingdom) | Details |
| ----Company:
Our Client is a large Contract Research Organisation (CRO) dealing in early phase clinical trials. They are looking for a Quality Assurance Manager to join their team in Croyden.
----Role:
The Quality Assurance Manager will report to the Research director and will be responsible for clinical audits ensuring the trials conform to the appropriate regulations, ICH-GCP, GMP... [Full Details] |
| Salary: Negotiable (35000 - 40000 £) |
| Regulatory And Drug Safety | Pharmacovigilance | Bedfordshire, Berkshire, Buckinghamshire, Hertfordshire,... | Details |
| This top 5 company who can boast a role in the development in 45 of top 50 products on the market are looking for an experienced pharmacovigilance professional to join the organisation as a regional head of pharmacovigilance to manage and lead projects in their jurisdiction.
The Role:
Provide management of the regional PPV Operations group, input in and leadership of... [Full Details] |
| Salary: Negotiable (45000 - 55000 £) |
| Regulatory And Drug Safety | Clinical Project Manager, Regulatory... | Warwickshire (United Kingdom) | Details |
| Accountabilities/Responsibilities:
For an assigned group of products:
-Assist in the preparation and submission of national, mutual recognition and decentralised regulatory dossiers.
-Prepare and submit variations to approved marketing authorisations.
-Prepare and submit applications to renew marketing authorisations.
-Liaise with regulatory agencies under supervision of senior officer or... [Full Details] |
| Salary: Negotiable (Up to 33000 £) |
| Regulatory And Drug Safety | Regulatory Affairs | Bedfordshire, Berkshire, Buckinghamshire, Hertfordshire,... | Details |
| Due to recent and further expansion there is now a need for an experienced regulatory professional to join the company. This exciting role will be ideal if you have particularly good previous CTA experience, you will also have previous supervisory experience and be able to show an ability to work with a high degree of autonomy.
The Role:
Provides regulatory affairs advice and support... [Full Details] |
| Salary: Negotiable (50000 - 55000 £) |
| Regulatory And Drug Safety | QA | East Midlands (United Kingdom) | Details |
| ----Company:
Our client is a major Pharmaceutical and Medical Device company based in East-Midlands/North UK. They are dedicated to providing cost-effective products to meet the growing needs of the healthcare industry in the UK. The company is currently looking for QA professionals to join their team.
----Role:
•To analyse and report results of raw materials and products
•To... [Full Details] |
| Salary: Negotiable (18000 - 25000 £) |
| Regulatory And Drug Safety | Pharmacovigilance | Surrey (United Kingdom) | Details |
| ----Company:
Our clients are one of the world’s leading pharmaceutical companies and have seven major therapy areas: Cardiovascular medicine, thrombosis, oncology, internal medicine, metabolic disorders, diseases of the central nervous system and vaccines.
----Role:
Objective of Role: To assist in the provision of an efficient pharmacovigilance service for marketed products... [Full Details] |
| Salary: Negotiable (25000 - 28000 £) |
| Regulatory And Drug Safety | Regulatory Affairs | Bedfordshire, Hertfordshire, London - Central,... | Details |
| Regulatory Affairs Manager
This top pharma company offers an unparalleled progression and has a strong presence globally. With a wide range of therapeutic areas already covered they are looking to recruit the right candidate to join their team as a Regulatory Affairs Manager.
KEY DUTIES AND RESPONSIBILITIES:
1. Initiate, manage and maintain operational activities in support of R&D... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Regulatory Affairs | London - Central, London - North, London - East, London -... | Details |
| A fantastic opportunity to join a Top independent oganisation as a Regulatory Affairs Manager. This company offers applicants unique opportunities to be involved and take their own approach to processes and systems so independent and ambitious candidates will be well suited. The client is almost entirely funded by the public with income from fundraising, investments and charitable activities.... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA, Drug Safety, Pharmacovigilance,... | London - Central, London - North, London - East, London -... | Details |
| Clinical Quality Assurance Officer
A rare opportunity to work for a leading global pharmaceutical company in a Quality Assurance Officer ( QA) role, this position offers the very highest level of professional’s development focusing on CNS trials.
Clinical Quality Assurance Officer
To ensure that systems with procedures that assure the quality of every aspect of clinical trials... [Full Details] |
| Salary: Negotiable (Up to 50000 £) |
| Regulatory And Drug Safety | Drug Safety, Pharmacovigilance | Berkshire, Hampshire, Oxfordshire, Surrey, London - South... | Details |
| This TOP 20 Global Pharmaceutical Company are now looking to recruit. They have an exciting product portfolio and a very healthy pipeline. Due to there continuous expansion there is a lot of opportunity for training and development and career progression.
They are now looking to recruit a Drug Surveillance Officer. You will have a life science degree and three years experience within... [Full Details] |
| Salary: Negotiable (Up to 35000 £) |
| Regulatory And Drug Safety | Drug Safety, Pharmacovigilance,... | 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 | Drug Safety, Pharmacovigilance | London - Central, London - North, London - East, London -... | Details |
| PHARMACOVIGILANCE MANAGER - HERTFORDSHIRE
This is a excellent opportunity to join a growing pharmaceutical company that operates on an international level. The position will participate in the management of the ongoing functioning of an effective regional Pharmacovigilance network. In addition, they will become therapeutic specialists and provide scientific review and input on documents... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Regulatory Affairs | Hampshire, Surrey (United Kingdom) | Details |
| An opportunity for a Regulatory Professional to gain some further experience with a TOP GLOBAL Pharmaceutical company. Your title will be Regulatory Compliance Associate - GCP and you will need to have experience within GCP Auditing.
Responsibilities:
You will be working in Global Consumer Healthcare on TOP brands. You will be based at the companies global innovation centre and will be... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA | Berkshire, Hampshire, Surrey (United Kingdom) | Details |
| International Quality Assurance Manager
We have an excellent opportunity that has arisen with a TOP global pharmaceutical company working to provide QA support and ensure that products are manufactured in accordance with Marketing/Manufacturing Authorisations and GMP guidelines. This role will report in to the Director of QA and is offering a competitive salary and benefits package. This is a... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | QA, Regulatory Affairs | Bedfordshire, Buckinghamshire, Essex, Hertfordshire... | Details |
| Manager, Regulatory Affairs, Submissions Compliance (QC)
An excellent opportunity to work with a top global Pharmaceutical company who are currently developing a number of diverse and exciting products. Working within this large company will be an fantastic opportunity to broaden your experience, enabling you to take your next step up the career ladder!
The position will be responsible... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Regulatory Affairs | East Sussex, Hampshire, Kent, West Sussex, Middlesex,... | Details |
| Senior Manager, Marketed Products - Regulatory Affairs
An excellent opportunity to work with a top global Pharmaceutical company who are currently developing a number of diverse and exciting products. Working within this large company will be an fantastic opportunity to broaden your experience, enabling you to take your next step up the career ladder!
Main Purpose of the Role:
•... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Regulatory Affairs | London - Central, London - North, London - East, London -... | Details |
| SENIOR MANAGER, REGULATORY INTELLIGENCE AND COMPLIANCE
An excellent opportunity to work with a top global Pharmaceutical company who are currently developing a number of diverse and exciting products. Working within this large company will be an fantastic opportunity to broaden your experience, and is a fantastic chance for you to take your next step up the career ladder!
ROLE... [Full Details] |
| Salary: Negotiable |
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