Jobs4 Drug Development device: click to go to Site Home Page
Jobs4 Drug Development logo: click to go to Site Home Page
Jobs4DD advert  : Clinical Professionals 1 TopJobs4DD advert  : PPD Top Banner
Latest news:
Filter your search for speciality and location requirements:
2_CSL-new-1-logo-2.jpg

Job vacancy list

Vacancies posted by: CSL Recruitment

Job Field: All Job Fields

Showing First Page | Next >> | Last Page
Showing 1 to 20 of 30
Job FieldGradeSpecialityRegionActions
Clinical ResearchAny GradeCRA, Clinical Study CoordinatorLancashire, 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 GradeClinical 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 & ContractsAny GradeProgrammer, Contracts & ProposalsBerkshire, 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 GradeClinical 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 ManagementAny GradeStatisticians, Data ManagementCambridgeshire, 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 SafetyAny GradeClinical 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 ManagementAny GradeStatisticians, Data ManagementManchester, 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 ManagementAny GradeStatisticians, Data ManagementManchester, 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 InformationAny GradeLaboratory 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 GradeClinical 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 ResearchAny GradeClinical 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 InformationAny GradeLaboratory 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 SafetyAny GradeClinical Project Manager, Drug SafetyBedfordshire, 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 InformationAny GradeLaboratory 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 SafetyAny GradeClinical 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 SafetyAny GradeClinical 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 GradeClinical 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 ResearchAny GradeCRA, Clinical Study CoordinatorBerkshire, 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 GradeClinical 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 SafetyAny GradeClinical 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
Showing First Page | Next >> | Last Page
Showing 1 to 20 of 30

Click buttons to view current vacancies

Clinical Research Jobs
CRM (Clinical Research Management) Jobs
IT & Data Management Jobs
Licensing & Contracts Jobs
Medical Information Jobs
Nurse Jobs
Physicians Jobs
Regulatory and Drug Safety Jobs
Testing & Analysis Jobs
Click here to join now
Jobs4DD advert  : Icon ClinicalJobs4DD advert  : Quintiles New RHSJobs4DD advert  : Clinical Professionals RightJobs4DD advert  : StelfoxJobs4DD advert  : PPDi BannerJobs4DD advert  : Chiltern