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| Job Field | Discipline | Region | Actions |
| Regulatory And Drug Safety | Clinical Project Manager | Hertfordshire (United Kingdom) | Details |
| We are currently looking for a Senior Quality Risk Specialist for an International Pharmaceutical company based in Hertfordshire, UK.
You will support risk assessments, collaborate with business partners, ensure the appropriate use of the Quality Risk Management system and ensure quality issues are addressed.
Main Duties;
• Provide overview on MA’s & CAPA’s
• Work as part of... [Full Details] |
| Salary: Negotiable |
| CRM (Clinical Research Management) | Clinical Project Manager | Any Location (Switzerland) | Details |
| Clinical Project Manager, Late Phase, Geneva / Switzerland
SUMMARY
Clinical Project Manager with significant experience of Late Phase Clinical Research (IIIb/IV) required for permanent role with specialist CRO based in the Geneva. You will be working on an exciting range of projects including peri-approval studies, outcomes research, post marketing, registry studies, safety surveillance and... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Clinical Project Manager | Any Location (Belgium, Germany) | Details |
| QP Pharmacovigilance and Drug Safety
An advancing Pharma company is now offering a new position within its organisation. The QP Pharmacovigilance position will play a key part between the Clinical Development, Quality and Medical Affairs team. The client holds a very successful pipeline benefiting from significant investment in its key product area.
You will be responsible for drug safety... [Full Details] |
| Salary: Negotiable |
| CRM (Clinical Research Management) | Clinical Project Manager | Hertfordshire, Middlesex (United Kingdom) | Details |
| Excellent position for a capable Project Manager who can aid and drive forward activities to support expansion of drug registration into wider markets. You will be working with ground breaking drug candidates and creating project plans, supporting operational group training and facilitating resourcing aspects alongside others in a similar role.
We are seeking candidates with solid project... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Clinical Project Manager | Any Location (Ukraine) | Details |
| Main Duties & Responsibilities:
- To act as a regulatory project manager for assigned clinical studies in any phase of development.
- Coordination and project management of worldwide CTA applications and CTA amendments in line with client expectations and allocated budget.
- Prepare, review and compile regulatory CTA applications, amendments, and end of trial notifications.
- Liaise... [Full Details] |
| Salary: Negotiable |
| CRM (Clinical Research Management) | Clinical Project Manager | Middlesex (United Kingdom) | Details |
| Our client is seeking people with good clinical R and D skills and the right team behaviours to join their international team. Twice named as one of the top 100 UK employers, this company has a strong pipeline and a friendly working environment.
The key responsibilities in this roleare:
Contribute to the design, content, and preparation of clinical protocols, amendments, consent forms,... [Full Details] |
| Salary: Negotiable |
| CRM (Clinical Research Management) | Clinical Project Manager | Any Location (United Kingdom) | Details |
| Our client develops medical products to assist in all aspects of wound healing. They are seeking an individual with the right characteristics to manage all global aspects of clinical development, including scientific investigation, protocol writing, KoL development, operations management, medical writing and product regulatory submission.
To be considered for the role, individuals must be... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Clinical Project Manager | Any Location (Belgium, Germany) | Details |
| COMPANY STATEMENT
This is a medium sized company with a friendly and good culture based on achieving great results through great individuals working in great teams. They are currently going through a very strong growth period following increase in sales from successful products. The drug safety /pharmakovigilanz department is expected to grow over the next ½ years and the drug safety quality... [Full Details] |
| Salary: Negotiable (45000 - 60000 £) |
| Regulatory And Drug Safety | Clinical Project Manager | Any Location (United Kingdom) | Details |
| We are currently looking for a Senior QA Manager for an company based in Berkshire, UK. We need an passionate and flexible person to provide auditing and Quality Assurance activities in order to assure that the systems processes and performance comply with applicable laws, regulations, SOPs, protocols and guidelines.
Main Duties-
•Deputise for the Senior Director for delegated projects... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Clinical Project Manager | Any Location (Switzerland) | Details |
| My client, a leading global pharmaceutical company are looking for a Senior Pharmacovigilance (PV) Auditor to join them in their HQ based in Switzerland.
As Senior Pharmacovigilance (PV) Auditor, you will apply expertise related to PV and good clinical practice (GCP) compliance auditing activities.
To be successful in this role you will have strong knowledge of;
• Drug... [Full Details] |
| Salary: Negotiable |
| CRM (Clinical Research Management) | Clinical Project Manager | Any Location (Belgium, Finland, France, Germany, Hungary,... | Details |
| The Director, Project Management (Endocrinology & Metabolic Diseases) provides strategic management as a Project Director across multiple projects and/or programs as well as the development of Project Management staff. The Senior Director will have a strong therapeutic career path providing strategic management with a broad focus in the therapeutic development of staff and function.
You can... [Full Details] |
| Salary: Negotiable |
| CRM (Clinical Research Management) | Clinical Project Manager | Any Location (France, Germany, Italy, Netherlands, The,... | Details |
| i3 brings a sharp therapeutic focus to clinical research, while providing a global reach. With offices worldwide and capabilities in more than 54 countries, we have the resources to launch clinical trials all over the world. As a UnitedHealth Group company i3 is part of a worldwide health care service organization that uses innovation, integrity and commitment to prepare for the future - and you... [Full Details] |
| Salary: Negotiable |
| CRM (Clinical Research Management) | Clinical Project Manager | Any Location (Singapore) | Details |
| The Clinical Project Manager manages the project team in the delivery of quality trial management services to achieve the agreed goals of the Customer and i3 research.
i3 brings a sharp therapeutic focus to clinical research, while providing a global reach. With offices worldwide and capabilities in more than 54 countries, we have the resources to launch clinical trials all over the world. As... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Clinical Project Manager | Any Location (Hungary) | Details |
| Main Duties & Responsibilities:
- To act as a regulatory project manager for assigned clinical studies in any phase of development.
- Coordination and project management of worldwide CTA applications and CTA amendments in line with client expectations and allocated budget.
- Prepare, review and compile regulatory CTA applications, amendments, and end of trial notifications.
- Liaise... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Clinical Project Manager | Any Location (Slovakia) | Details |
| The main duties & responsibilities:
- Track of status and progress of regulatory documentation.
- Review, edit and proofread regulatory documentation.
- Assist in preparation and review of labelling and other departmental documents.
- Support local marketing by means of timely and effective communication.
- Compile under supervision regulatory documents for submission.
- Participate as... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Clinical Project Manager | Any Location (Austria) | Details |
| Responsibilities:
• You will be responsible for development, preparation, and submission of applications and notifications to international regulatory agencies and government bodies
• You will provide input to product development projects and changes to existing products
• You will provide input to the development of regulatory strategies and obtaining regulatory approvals from... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Clinical Project Manager | London (Germany, United Kingdom) | Details |
| Considering becoming an interim? Or new to SEC recruitment?
The demand for flexible contract/interim professionals who can join an organisation over a short period and add value has grown and we are proudly leading the way in Interim provision.
I specialise in Drug Safety and Pharmacovigilance and would be interested in hearing from you and discussing possible contracting opportunties... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Clinical Project Manager | Any Location (France, Germany) | Details |
| Regulatory Affairs Specialist
LOCATION
Paris France, could be home based in France or Germany
COMPANY STATEMENT
Medical Device development company with a very strong reputation for expertise in medical device development. Although a fairly young company it is based on hiring highly experienced Medical device professionals who all bring their own experience and... [Full Details] |
| Salary: Negotiable (40000 - 45000 £) |
| CRM (Clinical Research Management) | Clinical Project Manager | Any Location (Switzerland) | Details |
| If you're a fan of winter sports this might be of interest to you!
A great opportunity to work in Basel on a 12 month contract in the translational medicine department of a major pharmaceutical company.
Ex-pat services are available to help ensure a seamless transition to living and working abroad.
The Clinical Trial Leader is responsible for the planning and implementation of all... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Clinical Project Manager | Cambridgeshire, London, Middlesex (United Kingdom) | Details |
| Our client is offering a great opportunity for a Drug Safety Associate to join their multidisciplinary team in the UK.
Duties and responsibilities:
-Triaging, collecting, monitoring, processing, and distributing adverse event reports (serious and non-serious Adverse Event(s) to the sponsor or regulatory authorities and project team within the specified timelines
- Duplication check and... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Clinical Project Manager | South Yorkshire (United Kingdom) | Details |
| Clinical Quality Assurance Auditor GCP GLP GCLP – CRO - £30,000+ and Excellent benefits
SUMMARY
There is now the opportunity for an experienced Quality Auditor to join this hugely successful organisation in a senior role within their UK operation. It is a strategically hands-on opportunity in their Quality assurance function and team and being the key point of contact for all Good... [Full Details] |
| Salary: Negotiable (20000 - 35000 £) |
| Regulatory And Drug Safety | Clinical Project Manager | Any Location (United Kingdom) | Details |
| Quality Assurance QA Associate Laboratory GLP - Contract Research Organisation – LONDON - £35,000 + Benefits
SUMMARY
This exciting new position is for an experienced Quality Assurance QA Associate who is looking for a challenging role within a growing organisation with involvement across the QA department and continual career progression. They offer an innovative product and are going... [Full Details] |
| Salary: Negotiable (30000 - 40000 £) |
| Regulatory And Drug Safety | Clinical Project Manager | West Sussex (United Kingdom) | Details |
| My client is one of the world's leading pharmaceutical companies. We are currently working with them in recruiting an Associate Director within their Health Economics and Outcomes Research group.
Job Description
- Execute HE&OR strategies that demonstrate overall product value (clinical and economic).
- Develop and integrate parameters necessary to demonstrate clinical, economic, and... [Full Details] |
| Salary: Negotiable |
| CRM (Clinical Research Management) | Clinical Project Manager | Any Location (Germany) | Details |
| Clinical Project Manager, Late Phase, GERMANY
Clinical Project Manager required for by Global CRO for Late Phase (Phase IIIb/IV) Project Management role based in Germany. You will be managing International post-marketing / approval studies across a range of therapy areas. The role can be based from home or from one of the company’s offices in Germany including Berlin, Frankfurt and... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Clinical Project Manager | Any Location (Switzerland) | Details |
| Pharmacovigilance Manager - Switzerland
My client, a leading pharmaceutical company are looking to recruit a Pharmacovigilance Manager to lead their Drug Safety team. This is a fantastic opportunity to join one of the world’s leading pharmaceutical companies.
As Pharmacovigilance Manager, you will be responsible for all aspects of safety related our clients products in early and late... [Full Details] |
| Salary: Negotiable |
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