| Job Field | Grade | Speciality | Region | Actions |
| 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 £) |
| CRM (Clinical Research Management) | Any Grade | Clinical Study Admin, Clinical... | Essex, Surrey, Middlesex (United... | Details |
| We are currently looking for candidateswho possess the skills below to fill an urgent contract for a leading Biotech
- BSc (LifeSciences) or Nursing Qualification
- Prior experience in oversight of clinical research vendors (CROs, central labs,
imaging vendors etc)
- Project planning experience including oversight of study deliverables, budgets,
and timelines
- Experience... [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... | Berkshire, Buckinghamshire,... | Details |
| To be considered for this role you must be confident and competent. You must have built a reputation within the industry or your current organisation on your ability to deliver, work flexibly and efficiently, and with the ability to overcome problems with solutions that work.
A background in neurology ( or dermatology )would be an advantage. Study start-up experience is vital, as is... [Full Details] |
| Salary: Negotiable |
| IT & Data Management | Any Grade | Statisticians, Data Management | Cambridgeshire, Hertfordshire (United... | Details |
| This is senior statistician position, and not a statistical programming role. Candidates must be able to demonstrate a thorough knowledge of statistical methodologies and be able to give practical examples of how they have applied these in a drug development programme across Phases I-III.
Key responsibilities are:
The Biostatistics team is therapeutic aligned, and you will need to be an... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Any Grade | Clinical Project Manager, Regulatory... | Cambridgeshire, Hertfordshire (United... | Details |
| The Role:
They are looking for a Senior Project Manager within International Regulatory Affairs division based in Cambridge. This is a full-time office based role, and you will be supporting senior management Regulatory Affairs in strategic planning, issue identification and resolution, and day-to-day business operations.
Experience Required:
- Ideally you will have cross-functional... [Full Details] |
| Salary: Negotiable |
| IT & Data Management | Any Grade | Statisticians, Data Management | Manchester, West Yorkshire (United... | Details |
| The role will involve the following:
- provision of expert statistical contributions to the design of clinical studies in a specific therapeutic area or area of expertise (e.g. clinical pharmacology, discovery medicine, health economics)
- reviewing risk assessment, decision-making processes (e.g. tollgate decisions, labelling)
- performing the statistical analysis of data from a series... [Full Details] |
| Salary: Negotiable |
| IT & Data Management | Any Grade | Statisticians, Data Management | Manchester, West Yorkshire (United... | Details |
| The role will involve the following:
- provision of expert statistical contributions to the design of clinical studies in a specific therapeutic area or area of expertise (e.g. clinical pharmacology, discovery medicine, health economics)
- reviewing risk assessment, decision-making processes (e.g. tollgate decisions, labelling)
- performing the statistical analysis of data from a series... [Full Details] |
| Salary: Negotiable |
| Medical Information | Any Grade | Laboratory Technician, Medical... | Essex, Hertfordshire, Middlesex... | Details |
| Skill & Experience Sought:
Pharmacists - Relevant experience in hospital clinical pharmacy or medicines information, and applicable experience in a Pharmaceutical Company Medical Information department.
Life Science graduates - relevant experience in a Pharmaceutical Company Medical Information department.
Experience in the Oncology area is highly advantageous although not... [Full Details] |
| Salary: Negotiable |
| CRM (Clinical Research Management) | Any Grade | Clinical Study Admin, Clinical... | Buckinghamshire, Oxfordshire,... | Details |
| Our Client one of the fastest growing pharmaceutical companies has a superb permanent opening for a capable Senior Medical Advisor ready for the next step. You must have expertise in supporting product launch and positioning in Europe and valid expertise in associated clinical development and study strategy to apply for this position. You will ideally have clinical expertise or understanding... [Full Details] |
| Salary: Negotiable |
| Clinical Research | Any Grade | Clinical Study Coordinator, Clinical... | Berkshire, Hampshire, Surrey (United... | Details |
| Lead CRAs, clinical researchers who have had control and responsibility for TMF inspection readiness will gain a wider understanding of this developing area from study planning to archiving. The role will suit someone who may have had or want audit duties and has a keen interest in establishing good control with vendors and globally within a major Pharma R&D environment.
CTAs with degrees are... [Full Details] |
| Salary: Negotiable |
| 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 |
| 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 | 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 |
| 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 |
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