In addition to viewing our Pharmacovigilance jobs, you may also wish to register now for other specialist medical recruitment services including Jobs by Email.
| Job Field | Discipline | Region | Actions |
| Testing & Analysis | Pharmacovigilance | Any Location (Russia) | Details |
| As a part of some of the best experts in the area of manufacturing of new medicaments you will provide continuous professional hands-on consultancy and expertise during the qualification, validation of master plan and start-up phases of a new sterile department for our product (plans, protocols, execution and reports).
The company is looking for an experienced consultant in the GMP area,... [Full Details] |
| Salary: Negotiable (90 - 120 £) |
| Regulatory And Drug Safety | Pharmacovigilance | 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 | 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 £) |
| Testing & Analysis | Pharmacovigilance | Berkshire (United Kingdom) | Details |
| Job Description –
Job Title: LTE and data transport and 3 g mobile /OSS Systems
Job Type Permanent
Windsor Berkshire
Summary:
My Client is looking for candidate with LTE and data transport and 3 g mobile /OSS Systems experience .
The role can be summarized as technical delivery management in a telecommunications software company. The role involves extensive travel and focuses on... [Full Details] |
| Salary: 50000 - 60000 £ |
| Regulatory And 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 | 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 |
| Testing & Analysis | Pharmacovigilance | Any Location (Switzerland) | Details |
| Analytical Development Chemist
My Client, a world leading pharmaceutical company, is looking for a talented individual to work as Analytical Development Chemist. The professional we are looking for has to be fluent in German and English.
You will lead the analytical development team, working on new analytical methods and validate them according to GMP guidelines and ICH guidelines. You... [Full Details] |
| Salary: Negotiable |
| Testing & Analysis | Pharmacovigilance | Any Location (Switzerland) | Details |
| My Client, a world leading pharmaceutical company, is looking for a talented individual to work as Pre-Clinical Research Scientist. The professional we are looking for has to be fluent in German and English.
Acting as study director and study personnel for non-clinical studies (GLP-studies according to GLPV SR 813.112.1 and non-GLP-studies), You will create study protocols and reports for... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Pharmacovigilance | London (United Kingdom) | Details |
| Senior Drug Safety Associate
Based in London
Permanent/Full Time
Salary - c£40,000 + benefits
This is an excellent opportunity to join an established CRO and work as Senior Drug Safety Associate
Job Requirements
•Lead and manage projects including the development of project specific safety reporting procedures and workflow and provide guidance to the team on the... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Pharmacovigilance | London (United Kingdom) | Details |
| Pharmacovigilance Scientist
Based in London
Permanent
This is a fantastic opportunity to work on a permanent basis for a well established organisation.
Job Requirements
•Processing of cases and SAEs
•Assist in writing aggregate report writing
•Ensuring that cases are processed within timelines
•Become the main lead within some projects
Candidate... [Full Details] |
| Salary: Negotiable |
| Testing & Analysis | Pharmacovigilance | Berkshire (United Kingdom) | Details |
| Job Description –
Job Title: Senior Systems Engineer
Job Type Permanent
Windsor Berkshire
Summary:
The role can be summarized as technical delivery management in a telecommunications software company. The role involves extensive travel and focuses on ensuring overall technical systems design and integrity of the software delivery.
The ideal candidate will have a proven track record... [Full Details] |
| Salary: 59000 - 60000 £ |
| Regulatory And Drug Safety | Pharmacovigilance | North Carolina (United States Of America) | Details |
| Job Category Pharmacovigilance
Primary Location North America-United States-North Carolina-Morrisville - McCrimmon
Description
The Manager, Pharmacovigilance (PVG) has overall responsibility for the planning, coordination and delivery of a group of Principal Safety Specialist, Senior Safety Specialists, and Safety Specialists, grouped by assigned projects and sponsors whenever it is... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Pharmacovigilance | North Carolina (United States Of America) | Details |
| Job Category Pharmacovigilance
Primary Location North America-United States-North Carolina-Wilmington
Description
The basic purpose and objective of this position is to provide safety support to the Safety and Medical Management Division, which includes safety database entry, Access and Excel database entry, scanning, quality control of scanned documents, report distribution internally... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Pharmacovigilance | North Carolina (United States Of America) | Details |
| Job Category Pharmacovigilance
Primary Location North America-United States-North Carolina-Wilmington
Description
The basic purpose and objective of this position is to provide safety support to the Safety and Medical Management Division, which includes safety database entry, Access and Excel database entry, scanning, quality control of scanned documents, report distribution internally... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Pharmacovigilance | Berkshire, Buckinghamshire, Hampshire, London, Surrey,... | Details |
| Job summary
• Top 10 Pharmaceutical company
• Long term rolling contract
• Permanently employed by Chiltern
• Office based in Surrey
Job Background
The RS (Resourcing Solutions) department of Chiltern International acts in a similar way to that of a staffing solutions provider. The department is currently seeking a Surveillance Associate / Scientist to work for our client,... [Full Details] |
| Salary: Negotiable (28000 - 34000 £) |
| Regulatory And Drug Safety | Pharmacovigilance | Bedfordshire, Berkshire, Buckinghamshire, Hampshire,... | Details |
| Pharmacovigilance Coordinator
Berkshire
12 month fixed term contract
Competitive Salary, Plus Benefits
This is a 12 month fixed term contract working as a Pharmacovigilance Coordinator based in Berkshire, this is an excellent position to develop a career within pharmacovigilance.
Key Responsibilities
•Centralizing Serious Adverse Event Reports
•Working with deadlines for... [Full Details] |
| Salary: Negotiable |
| Testing & Analysis | Pharmacovigilance | Berkshire (United Kingdom) | Details |
| Contract position-Test Consultant - Netcool Expert
My Client is currently seeking a Test Consultant who is an expert in Netcool for a contract role working in Berkshire for one of our Telecoms clients.
We are seeking a Test Consultant with OSS software testing background and who can lead and co-ordinate the testing of software development and integration services on client site.
We are... [Full Details] |
| Salary: Negotiable (400 - 401 £) |
| Regulatory And Drug Safety | Pharmacovigilance | Dublin (Ireland) | Details |
| Our client is a leading global biopharmaceutical company. They are currently seeking a full time Senior QA Specialist (GMP) within their Supplies/Manufacturing division to be based on site in Dublin, Ireland.
JOB ROLE:
To ensure that all appropriate batch related documents and finished product packs are available from the contractors/suppliers to enable the release of products for sale or... [Full Details] |
| Salary: Negotiable |
| Testing & Analysis | Pharmacovigilance | Hertfordshire (United Kingdom) | Details |
In this position you will be aiding in the design of capsules, tablets and controlled release technologies for formulation development and clinical trials. You will spend your time working either in the laboratory or processing in the pilot plant.
Responsibilities:
- Supporting formulation activities from small-scale experimental work through to pilot scale... [Full Details] |
| Salary: Negotiable (Up to 1 £) |
| Testing & Analysis | Pharmacovigilance | Any Location (Belgium) | Details |
| Job description:
• Qualification reviews, including all reviews related to production and validation
• Ensure test document preparation and/or reviews for R&D projects and production
• Oversee system testing activities
• Management of corrective actions, follow up and audits
• Review all validation and design verification activities
Your profile:
• Master degree in... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Pharmacovigilance | North Carolina (United States Of America) | Details |
| Job Category Pharmacovigilance
Primary Location North America-United States-North Carolina-Wilmington
Description
The Safety Specialist is responsible for coordinating and performing adverse event data entry, coding and assessment of adverse events, case review, follow up with reporter and/or associated HCP, tracking of reports, and regulatory reporting activities. The Safety Specialist... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Pharmacovigilance | North Carolina (United States Of America) | Details |
| Job Category Pharmacovigilance
Primary Location North America-United States-North Carolina-Wilmington
Description
The Safety Specialist is responsible for coordinating and performing adverse event data entry, coding and assessment of adverse events, case review, follow up with reporter and/or associated HCP, tracking of reports, and regulatory reporting activities. The Safety Specialist... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Pharmacovigilance | Buckinghamshire (United Kingdom) | Details |
| JOB ROLE:
The Principal Medical Writer will assist with the authoring of regulatory documents for clinical research, including clinical study reports, clinical summary sections of common technical documents, investigator brochures, protocols, and other clinical documents.
PRINCIPAL RESPONSIBILITIES include:
• Compiles and assembles components of clinical documents in accordance with... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Pharmacovigilance | North Carolina (United States Of America) | Details |
| Job Category Pharmacovigilance
Primary Location North America-United States-North Carolina-Morrisville - 1800 Perimeter
Description
The Safety Specialist is responsible for coordinating and performing adverse event data entry, coding and assessment of adverse events, case review, follow up with reporter and/or associated HCP, tracking of reports, and regulatory reporting activities. The... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Pharmacovigilance | Any Location (Switzerland) | Details |
| Local Safety Specialist- Switzerland
Description:
A Swiss subsidiary of a leading internationally Pharma company are looking for a motivated person to take up the position of Local Safety Specialist.
The Local Safety Officer is responsible for pharmacovigilance but additionally responsible for quality assurance, complaint handling and preparation of SOPs; training responsibilities and... [Full Details] |
| Salary: Negotiable |
Site by Redder