Clinical Trials Jobs in Surrey
Find Clinical Trials jobs in Surrey within the Materials / Scientific industry. Search and apply today.
Alternatively, register with Jobsite, upload your CV and let Materials / Scientific recruiters in Surrey find you. Once registered, we can send you an email job alert each time a new Clinical Trials job becomes available.
You are here: Jobs > Materials / Scientific > Clinical Trials > Surrey
Sort by:
Senior CRA - UK Clinical Trials
- Salary:
- £35k - £45k pa
- Location:
- Camberley, Croydon, Guildford, Kingston Upon Thames, Richmond Upon Thames, Surrey
- Job Type:
- Permanent
- Date Posted:
- 27-May-2012 18:29Add to My Shortlist
An excellent opportunity is available to join a successful European based Clinical Research Organisation CRO. They require a Senior CRA or Principal CRA to start up and Lead their UK clinical trials. As their Senior Clinical Research Associate SCRA you will be setting up the trials and assisting in the site selections. You will ultimately responsible for the conduct and reporting of the trials. You will act as the key contact with the sponsors, investigator and study teams. My client is looking...
Senior Regulatory Officer
- Salary:
- £42k - £43k pa + Full Benefits package
- Location:
- Camberley
- Job Type:
- Permanent
- Date Posted:
- 28-May-2012 16:53Add to My Shortlist
As the global leader in the ophthalmic marketplace, we are proud to meet the eye care needs of millions of people worldwide. For over 60 years, we have developed, produced and marketed the most advanced products available in ophthalmology. Dedicated to the provision of not only the highest quality eye care products, but to also making significant contributions towards the... our senior regulatory experts, you will prepare and submit high quality and timely regulatory applications to the MHRA/IMB, take the lead in co-ordinating activities with regulatory officers and act as a key UK/Ireland contact. The successful candidate will be able to : -Work autonomously in the compilation and submission of Clinical Trial Applications, Marketing Authorisation Applications, Variations, Renewals, Product Information changes and responses to Requests for Further Information, within specified timelines and to agreed quality standards -Pursue maintenance activities for assigned portfolio to ensure ongoing compliance with local and EU regulations and company procedures -Facilitate discussions at senior level with regard to...
Regulatory Affairs Director
- Salary:
- Competitive Salary
- Location:
- Surrey
- Job Type:
- Permanent
- Date Posted:
- 26-May-2012 00:00Add to My Shortlist
Primary Goal Responsible for directing all regulatory activities and developing and implementing strategies for timely approvals of Phase I through Phase IV clinical trial applications; counselling and overseeing regulatory teams; ensuring timely preparation and submission of regulatory documentation to European and international drug regulatory authorities; ensuring the quality, content and format of regulatory submissions; and interacting with regulatory agencies, project team members and development partners. Key Responsibilities & Critical Objectives Assist in the new...
Director, Site Start-Up & Regulatory
- Salary:
- Negotiable
- Location:
- Camberley
- Job Type:
- Permanent
- Date Posted:
- 25-May-2012 14:58Add to My Shortlist
Responsible for one or multiple regions. Directs the development, implementation, and analysis of work within a broad area for newly awarded studies, including site activation, regulatory, submissions, site contracts, and/or regulatory records. Contributes to the business development process by reviewing proposals and attending client meetings. Ensures fulfillment of customer requirements and compliance with related regulations. Ensures continuous improvement of quality... within the Company which lead to greater efficiencies or competitive advantages over other companies. Other Responsibilities: Performs other work-related duties as assigned. Minimal travel may be required (up to 25%). Skills & Attributes BS degree in Pharmacy, other health-related area, or equivalentcombination of education and experience. Advanced degree preferred. Extensive Clinical Trial experience. Significant experience managing teams of clinical research staff. Sales experience preferred. Strong knowledge of clinical research management processes. Understanding of the needs of countries and the ability to work across geographic regions. Strong CRO operational experience with a track record in project management working in an international or global...
Senior Regulatory Affairs Officer
- Salary:
- 35000
- Location:
- Surrey
- Job Type:
- Permanent
- Date Posted:
- 26-May-2012 00:00Add to My Shortlist
You will be working in close collaboration with Manufacturing sites, Corporate Regulatory Affairs, EURMEA Regulatory Affairs, Marketing Managers and Medical Safety, the Senior Regulatory Affairs Officer will prepare and submit high quality and timely regulatory applications to the MHRA/IMB, coordinate activities with Regulatory Affairs Officers and act as key UK/Ireland contact within regional regulatory organisation. Following licence submission, the Senior Regulatory Affairs Officer will be in regular contact with the MHRA/IMB, responding to questions and ensuring progress leading to a successful conclusion. Your Areas of Responsibility will include: *Work autonomously in the compilation and submission of Clinical Trial Applications, Varia-tions, Renewals, Product Information changes and responses to Requests for Further Infor-mation, within specified timelines and to agreed quality standards. *Participate in the preparation of registration dossiers and project manage local Marketing Authrorisation Applications as well as other regulatory initiatives. *Pursue maintenance activities for assigned portfolio to ensure ongoing...
Senior EU Study Manager (Oncology)
- Salary:
- On Application
- Location:
- Berkshire, Buckinghamshire, Hertfordshire, Surrey, London, Middlesex
- Job Type:
- Permanent
- Date Posted:
- 24-May-2012 09:16Add to My Shortlist
JOB SUMMARY: Senior Study Management of Phase II and Phase III Oncology studies according to ICH guidelines in support of the clinical strategies defined in the Integrated Development Plan (IDP) as they relate to European specific responsibilities. Support of Phase I trials may also be required. Office based from London HQ. BACKGROUND: Expanding Global Pharmaceutical Company EU HQ based in... conducting clinical studies, which includes writing basic study protocols; managing study conduct, including oversight of CROs/other vendors; identifying and resolving study site issues; managing the study budget; and study closeout. QUALIFICATIONS / EXPERIENCE REQUIRED: * Bachelors Degree preferably in Life Sciences, or R.N., or international equivalent. * 3+ years of clinical trial management, Study Manager / Project Manager, experience including accumulation of one year of monitoring experience required (either in a pharmaceutical company or clinical research organization). * 1+ year of European clinical trial management * Demonstrated ability to manage clinical trials * Superior communication skills: written, oral, interpersonal and presentation * Excellent problem...
Pharmacovigilance and Medical Review Manager
- Salary:
- On Application
- Location:
- Berkshire, Buckinghamshire, Surrey, London
- Job Type:
- Permanent
- Date Posted:
- 25-May-2012 09:02Add to My Shortlist
JOB SUMMARY We are seeking to appoint a Pharmacovigilance and Medical Review Manager who will report directly to the Director of their local R&D structure. Covering the UK, the Pharmacovigilance and Medical Review Manager will assist in all aspects of local Medicinal Safety, in accordance with applicable regulatory requirements, guidelines, laws, and Servier quality standards and practices and in close... a leading French independent research based organisation specialising in ethical pharmaceuticals. Servier UK's head office is located in Wexham Springs, Buckinghamshire, at the heart of the UK pharmaceutical industry's cluster in the Thames Valley. PRIMARY DUTIES Ensure all safety reports are managed in compliance with ICH and GCP guidelines for clinical trials and marketed products * Communicates information relating to medicinal safety to Global PV in France, and other internal departments, for clinical trials and marketed products. * Assist in safety management activities with external partners * Actively participates in the maintenance of PV Quality management system> * Coordinates Medical Review for our...
Clinical Research Physician - Oncology, UK
- Salary:
- Excellent + Benefits
- Location:
- Berkshire, Buckinghamshire, Oxfordshire, Hampshire, London, Surrey, Uk
- Job Type:
- Any
- Date Posted:
- 29-May-2012 00:00Add to My Shortlist
Clinical Research Physician - Oncology My client, a leading pharmaceutical organisation with an international presence are looking to recruit a pharmaceutical physician with a background in Oncology at either Associate Director or Director level. Role Detail: Working in a Uk-based role, but as part of a global team, you will be responsible for the management and development of PI -... This is a permanent, office-based role with some international travel when required. To Apply: Please call Toby Ferguson at Only Medics on +44 (0) 1189 522799 or e-mail your CV to toby@onlymedics.com. All applications will be held in absolute confidence. Keywords: medic physician doctor research physician medical affairs clinical development clinical trials pharmacovigilance drug safety GMC Phase I Phase II Phase III Oncology Haematology Hematology Onco-Haematology Haemato-Oncology Cancer Berkshire Buckinghamshire Bedfordshire Hampshire Hertfordshire Middlesex London Surrey UK anywhere re-locate
Paediatric Research Nurse (Basingstoke and Dublin)
- Salary:
- Up to £32,000
- Location:
- Hampshire, Berkshire, Middlesex, Surrey, Dublin, Kildare, Wicklow, Meath
- Job Type:
- Permanent
- Date Posted:
- 30-May-2012 00:00Add to My Shortlist
PAEDIATRIC RESEARCH NURSE (SALARY: UP TO £32,000) (BASED IN: BASINGSTOKE AND DUBLIN) We are looking for two Full Time experienced paediatric clinical research nurse ( band 7) to work within a busy Paediatric Haematology department in Basingstoke and Dublin. The post is for 6 months in the first instance and is an excellent opportunity to be part of a rapidly growing organisation. The successful candidate will be experienced in performing and managing all aspects of clinical trial work within an investigator site and will be expected to work across Phase II-IV trials (both commercial and investigator led) in paediatric haematology. Qualifications, Education & Experience * RGN/RN Paediatric essential registered on the NMC register * Qualified for at least 5 years * First degree desirable * ICH-GCP training...
CRA South East England
- Salary:
- £28k-£45k
- Location:
- London, Brighton, West Sussex, Surrey, Buckinghamshire, Bedfordshire, Berkshire, Hertfordshire, Essex, Kent
- Job Type:
- Permanent
- Date Posted:
- 29-May-2012 09:08Add to My Shortlist
Job Summary: A dynamic CRO has a superb opportunity available for an experienced CRA working within large Cardiology and Oncology focused projects. Requirements: This truly international organisation has won a number of new projects and for this reason is looking to expand the affiliate office based in the south of England. Within this position you will monitor the progress of Cardiology and Oncology trials at investigative sites, and ensures that clinical studies are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements. Main Responsibilities: * Implements and monitors clinical trials to ensure sponsor and investigator requirements are met and are compliant with applicable local regulatory requirements and ICH guidelines * Mentors junior level CRAs and serves as a point of contact for new employees * Working largely on Cardiology trials at least for the immediate future * Visits sites to...
Biometrics Team Leader
- Salary:
- On application
- Location:
- London, Buckinghamshire, Oxfordshire, Hampshire, Berkshire, Surrey, Middlesex
- Job Type:
- Contract/Interim
- Date Posted:
- 30-May-2012 00:00Add to My Shortlist
BIOMETRICS TEAM LEADER (BASED IN: LONDON) (SALARY: ON APPLICATION) The is a new and exciting opportunity for a Biometrics Team Leader (Data Manager), to join an expanding company involved in Phases I-IV trials including Pharmacokinetic studies in patients and healthy volunteer studies. Initially a 6 Month Contract, working 3 days per week, based in the London area. As Biometrics Team Leader, you will be responsible for ensuring that all data management and statistical activities are conducted in accordance with the clinical trials legislation and guidelines. You will manage, co-ordinate, oversee and deliver all data management and statistical activities and provide leadership and management of personnel associated with these activities. MAJOR RESPONSIBILITIES *To act as the primary contact for data management, statistics, monitoring and regulatory personnel (the Team) in terms of Biometrics *To...
Senior EU Study Manager (Oncology)
- Salary:
- Competitive Daily Fee
- Location:
- Berkshire, Buckinghamshire, Hertfordshire, Surrey, London
- Job Type:
- Contract/Interim
- Date Posted:
- 25-May-2012 14:30Add to My Shortlist
Benefits: Competitive Daily Fee / PAYE JOB SUMMARY Senior Study Management of Phase II and Phase III Oncology studies according to ICH guidelines in support of the clinical strategies defined in the Integrated Development Plan (IDP) as they relate to European specific responsibilities. Support of Phase I trials may also be required. Office based in London. BACKGROUND Expanding Global Pharmaceutical... conducting clinical studies, which includes writing basic study protocols; managing study conduct, including oversight of CROs/other vendors; identifying and resolving study site issues; managing the study budget; and study closeout. QUALIFICATIONS / EXPERIENCE REQUIRED: * Bachelors Degree preferably in Life Sciences, or R.N., or international equivalent. * 3+ years of clinical trial management, Study Manager / Project Manager, experience including accumulation of one year of monitoring experience required (either in a pharmaceutical company or clinical research organization). * 1+ year of European clinical trial management * Demonstrated ability to manage clinical trials * Superior communication skills: written, oral, interpersonal and presentation * Excellent problem...
(Senior)European Medical Director CNS
- Salary:
- 80 - 100K GBP
- Location:
- England, London, Berkshire, Hampshire, Southampton, Basingstoke, Reading, Guildford, Bracknell, France, Netherlands, Germany, Belgium, Switzerland
- Job Type:
- Permanent
- Date Posted:
- 28-May-2012 18:17Add to My Shortlist
Medical Director (Neurologist) Barrington James is currently working with one of the world's largest and most respected pharmaceutical partners to source a Senior Medical Director for the CNS area of the business. This position has come through expansion and business demands of the CNS therapeutic area. We are currently hiring for a Medical Director, Senior Medical Director. The position offers... the marketplace. Work closely on evaluation and prioritisation of study opportunities within our CNS therapeutic area. Provide medical input and assistance in the feasibility discussions relating to specific study projects. Develop, review and revise protocols, case report forms, medical responsibility plans, adverse event reporting plans, training materials, analysis plans design, clinical trial reports and new drug applications. Participate in the continious process improvement activities across the business. Education/Qualifications * Medical Doctor (GMC required for the UK) with postgraduate training or equivalent experience in Neurology (preferred) * Knowledge of drug development process and extensive experience in clinical research * Ability to represent the...
Senior Clinical Pharmacologist
- Salary:
- £Negotiable + Benefits
- Location:
- London, Berkshire, Hampshire, Hertfordshire, Surrey, Middlesex, Essex, South East England
- Job Type:
- Any
- Date Posted:
- 24-May-2012 14:40Add to My Shortlist
Senior Clinical Pharmacologist Central London - Office Based £Neg dependent upon experience A fantastic opportunity has arisen at a highly successful global pharmaceutical company. You will be joining an organisation that specialises in marketing a diverse portfolio of products worldwide and this role has been created to contribute substantially to Clinical Pharmacology. You will look at the protocol development of... Senior Director The successful candidate will ideally have: *Ph.D or international equivalent *At least 3 years experience of PK/Clin Pharm experience in Pharmaceutical R&D, CRO or other relevant experience *Degree is expected in relevant scientific area e.g. Pharmacology, Pharmacokinetics, Pharmacodynamics, etc. *Experience in designing PK and implementing PK aspects of clinical trials or experience in Clin Pharm trial design *Good grasp of PK/PD evaluation techniques *Experience of writing PK or Clinical Pharmacology sections in clinical study reports This is a great time to be joining a prestigious company that really looks after its employees and are always recruiting due to continued success....
Study Physicians
- Salary:
- On Application
- Location:
- Cambridgeshire, Bedfordshire, Berkshire, Buckinghamshire, Essex, Hertfordshire, Surrey, London
- Job Type:
- Permanent
- Date Posted:
- 25-May-2012 09:09Add to My Shortlist
Benefits: Good basic salary, pension, holiday etc. JOB SUMMARY An excellent opportunity to move into the pharmaceutical industry and develop your career in early clinical research in this fast growing and innovative company working on antivirals and vaccines. BACKGROUND Our client is a fast-growing, innovative Contract Research Organisation specialising in the conduct of respiratory viral challenge clinical trials (Phase I and II). The company has pioneered a novel clinical trial Human Challenge model which allows their customers to gain valuable insight into their vaccines and anti-viral products in a fraction of the time it takes using standard field based clinical studies. PRIMARY DUTIES Reporting to the Head of Clinical...