| Job Field | Grade | Speciality | Region | Actions |
| Medical Information | Any Grade | Laboratory Technician, Medical... | Surrey, Middlesex (United Kingdom) | Details |
| The position is also to provide medical and scientific support and expertise to healthcare professionals and professional bodies through scientific communications and to facilitate a medical and scientific bridge between the client and the healthcare community.
Role Responsibilities:
Sign-off and approval of marketing materials or activities
Provision of medical insight and expert... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Any Grade | Clinical Project Manager, Drug Safety | Bedfordshire, Northamptonshire,... | Details |
| Key duties:
Receive details of spontaneous adverse events via telephone, letter or e-mail
Report details to the central case processing group within defined time frames
Ensure appropriate levels of follow-up with reporters to fulfil all legal and regulatory requirements
Ensure all appropriate reports are distributed to regulatory authorities, Ethics Committees and investigators within... [Full Details] |
| Salary: Negotiable |
| Medical Information | Any Grade | Laboratory Technician, Medical... | Berkshire, Middlesex (United Kingdom) | Details |
| A superb opportunity to diversify your knowledge of medical information, scientific advice, claim support or corporate compliance within a wider FMCG environment working for a household name which inspires confidence and leads the field in several Health & Beauty Care and luxury product areas.
We'd like to attract candidates who have an eye for detail and commercial acumen/flair for our... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Any Grade | Clinical Project Manager, Regulatory... | Bedfordshire, Cambridgeshire, Essex... | Details |
| The role will be responsible to develop and implement regional regulatory strategies to expedite global drug development and registration and manage the execution of regional strategy, communications and submissions. You will have expertise on regional regulatory requirements and precedence.
The ideal candidate must have significant experience of working with the Centralised procedure as well... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Any Grade | Clinical Project Manager, Regulatory... | Surrey, Middlesex (United Kingdom) | Details |
| We are seeking candidates with solid regulatory management skills in R&D or product licensing. Current understanding of pharmaceutical product development in EU is essential to allow swift adaptation to in this role.
This role is a senior management role and will demand skill in negotiating with peers and managers across alldisciplines involved in making and maintaining regulatory... [Full Details] |
| Salary: Negotiable |
| IT & Data Management | Any Grade | Data Management, Clinical Data... | Cheshire, Manchester (United Kingdom) | Details |
| The company is internationally recognised as being at the forefront of innovation, technology and market penetration, with it's core values recognizing the importance of customer satisfaction, environmental awareness and the value of its employees. The succesful candidate will have the chance to work alongside top professionals within the industry whilst gaining experience that is universally... [Full Details] |
| Salary: Negotiable (18000 - 22000 £) |
| CRM (Clinical Research Management) | Any Grade | Clinical Study Admin, Clinical... | Berkshire, Buckinghamshire,... | Details |
| The open permanent role will suit competent self starters who are satisfied to work at this level and function as a support for the Program Leads but not take the helm personally. Maturity, breadth of experience and skilled team playing ability are key to success through this busy period of change; there is good scope for developing knowledge across Phases as well as new molecules come into the... [Full Details] |
| Salary: Negotiable |
| Clinical Research | Any Grade | CRA, Clinical Study Coordinator | Lancashire, Manchester (United... | Details |
| The role is for an office based Clinical Research Associate to support and work alongside the Clinical Project Manager on a number of ongoing studies within the department. This will involve:
Helping mange site communication issues and monitor recruitment.
Assisting with project specific management.
Assuming an ambassadorial role to facilitate communication with sites.
Assists the CTA in... [Full Details] |
| Salary: Negotiable (25000 - 30000 £) |
| Clinical Research | Any Grade | CRA, Clinical Study Coordinator | Berkshire, Buckinghamshire,... | Details |
| Our client is a pharmaceutical company with novel products in ophthalmology and neurology. Based in Bucks, with good transport links,this role is an entry in to clinical operational project management.
To be considered for this role you must have:
- At least a BSc degree
- clinical monitoring experience in the EU
- a good understanding of all regulatory requirements for clinical... [Full Details] |
| Salary: Negotiable |
| Licensing & Contracts | Any Grade | Programmer, Contracts & Proposals | Berkshire, Buckinghamshire,... | Details |
| Duties:
Responsible for the logistical tasks associated with the preparation, collation and review of the regulatory document submission package.
Ensures distribution of draft essential documents to the selected sites. Responsible for drafting and reviewing of Study ICF.
Responsible for the developmentof the Country-specific Informed Consent templateby adapting the Study ICF templates with... [Full Details] |
| Salary: Negotiable (28000 - 30000 £) |
| CRM (Clinical Research Management) | Any Grade | Clinical Study Admin, Clinical Project... | Any Location (Switzerland) | Details |
| Our client's studies are not one size fits all and each must be designed and managed in a way that meets its specific purpose(s). Regulatory bodies are increasingly asking for long-term follow-up data on new medical products, whether it is a study of safety, benefit-risk management, outcomes and health economics, clinical and cost effectiveness, or quality.
Project Manager / Senior Project... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Any Grade | Clinical Project Manager, Regulatory... | Essex, Middlesex (United Kingdom) | Details |
| Responsibilities:
Use expertise in IE markets to provide input into product strategy for the IE region
Preparation of International Market Applications for new products
Review of post-marketing variations (labelling and CMC)
Generation of responses to agency questions. This includes:
Manage execution of product strategies for assigned MAA and variations
Interface with regional... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Any Grade | Clinical Project Manager, Regulatory... | Essex, Surrey, Middlesex (United... | Details |
| Our Client, a leading Biotech company, is currently recruiting additional Regulatory Managers. You will be responsible for developing and implementing effective regulatory strategies for assigned projects enabling the development and registration of the company's commercial product portfolio in the Middle East/Africa; Non-EU Central/Eastern Europe; Asia/Pacific and Latin America. As the lead... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Any Grade | Clinical Project Manager, Regulatory... | Essex, Surrey, Middlesex (United... | Details |
| Responsibilities:
Use expertise in IE markets to provide input into product strategy for the IE region
Preparation of International Market Applications for new products
Review of post-marketing variations (labelling and CMC)
Generation ofresponses to agency questions. This includes:
Manage execution of product strategies for assigned MAA and variations
Interface with regional regulatory,... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Any Grade | Clinical Project Manager, Regulatory... | Bedfordshire, Cambridgeshire, Essex... | Details |
| The role will be responsible to develop and implement regional regulatory strategies to expedite global drug development and registration and manage the execution of regional strategy, communications and submissions. You will have expertise on regional regulatory requirements and precedence.
The ideal candidate must have significant experience of working with the Centralised procedure as well... [Full Details] |
| Salary: Negotiable |
| CRM (Clinical Research Management) | Any Grade | Clinical Study Admin, Clinical Project... | 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) | Any Grade | Clinical Study Admin, Clinical Project... | 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 |
| Medical Information | Any Grade | Laboratory Technician, Medical... | East Sussex, Hampshire, Surrey (United... | Details |
| A first-in-class therapy that offers convenient subcutaneous administration using a pre-filled syringe formulation for the treatment of Hereditary Angioedema
an enzyme replacement therapy for the treatment of Fabry disease
a treatment for Gauchers disease)
The individual will raise awareness of these highly specialised drugs through the explanation of critical data to clinicians and a wider... [Full Details] |
| Salary: Negotiable |
| Clinical Research | Any Grade | Clinical Study Coordinator, Clinical... | Berkshire, Hampshire, Surrey (United... | Details |
| Main Duties:
Provide efficient clinical trials administrative support across Phase II - IV
Assist with accurate Clinical Trials Management System data entry and reporting
Assist with clinical document generation, review and revisions.
Attend study team meetings, responsible for production of internal meeting Agendas and Minutes in accordance with department best practices, under the... [Full Details] |
| Salary: Negotiable (175 - 185 £) |
| Medical Information | Any Grade | Laboratory Technician, Medical... | Essex, Hertfordshire, Middlesex... | Details |
| We're looking for candidates who meet the following criteria. A full job description is available on request.
- Medical Degree. Registered with GMC or other similar regulatory body
- Postgraduate Qualification (e.g.. Membership of a Royal College, PhD) desirable but not essential
- Adequate clinical and industry experience in medical affairs, preferably in CNS
- Sufficient experience in... [Full Details] |
| Salary: Negotiable |
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