Clinical Trials Jobs in Hertfordshire
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Associate, Clinical Trial Supplies
- Salary:
- On Application
- Location:
- Hertfordshire, London, Middlesex, Buckinghamshire
- Job Type:
- Permanent
- Date Posted:
- 26-May-2012 00:00Add to My Shortlist
JOB SUMMARY: To coordinate, under supervisory direction, IMP packaging, labeling, distribution and accountability activities contributing to the on-time delivery of quality-driven clinical supplies. To collaborate with clinical supply team colleagues and external vendors in the creation of value within the overall clinical development process. PRIMARY DUTIES: Main duties/responsibilities: * Coordinate, under supervisory direction, IMP packaging and labeling activities * Work... study team * Strong organizational and analytical skills, developing ability to work semi-autonomously * Good basic vendor management skills * Strong verbal/written communication and interpersonal skills, especially in the area of relationship management * Proficiency in software applications (Word, Excel, Powerpoint and database management) * Ability to travel (10%) KEYWORDS: Clinical trials supplies, IMP packaging, labeling, distribution TO APPLY: For a confidential discussion please telephone Omar de Bary at AXESS Limited on 020 8560 2300. To apply, please send your CV to jobs@axess.co.uk quoting reference 5184 . Only candidates with EU work authorisation will be considered. ABOUT AXESS: AXESS has been operating...
Manager Clinical Operations and Compliance, SOCS CFU
- Salary:
- On Application
- Location:
- Hertfordshire, London
- Job Type:
- Permanent
- Date Posted:
- 26-May-2012 00:00Add to My Shortlist
BENEFITS: Flexibility to work from home, pension, bonus JOB SUMMARY: Our client is a top tier pharmaceutical organisation based in Hertfordshire. This is a unique role which will combine your knowledge of Clinical Operations, Drug Safety and implementing and managing process. You have strong leadership capabilities with the ability to provide direction for these processes through direct line management of... efforts or inefficient processes. The manager will escalate and identify processes/issues and inform or request appropriate intervention by the Associate Director, Clinical Operations in a proactive manner. The Manager will also collaborate with IT to address any technical/database related issues. * Measure of success would include a positive impact on clinical trial timelines and/or controlled document, training, TMF or SUSAR issues. In addition, establishing innovative methods to streamline or combine activities which facilitate the quality of study trial documentation QUALIFICATIONS / EXPERIENCE REQUIRED: A bachelors in Science or health related discipline. KEYWORDS: Study Trial Administrator, CRA, SCRA, Senior CRA, Drug Safety, Clinical...
UK- Clinical Research Associate- Oncology
- Salary:
- On application
- Location:
- Stevenage, Hertfordshire, England
- Job Type:
- Permanent
- Date Posted:
- 25-May-2012 00:00Add to My Shortlist
Novella Clinical is a global full service eCRO, committed to providing an outstanding service to our client's as well as our employees. We focus on providing excellent training and career development opportunities, encouraging growth from within our talented work force. Our parent company is one of the World's leading not profit research organisations, and you will be joining a passionate... ICH GCP Perform SDV Query resolution Establish drug compliance Monitor and follow up AEs and SAEs Produce detailed accurate and timely visit reports Provide reports and feedback to Clinical Project Manager regarding; Patient screening Patient enrolment Data Queries Study progress Centre and study problems Adverse Events SAEs Organise and track clinical trial supplies including drugs, CRFs, diary cards, consent forms Organise and track investigator payments Provide study updates to regulatory bodies To be considered for this position you will be required to have a science degree or equivalent, be able to display a clear understanding of the drug development process, be familiar...
Associate Director Clinical Operations Neuroscience
- Salary:
- On Application
- Location:
- Cambridgeshire, Essex, Hertfordshire, London, Middlesex
- Job Type:
- Permanent
- Date Posted:
- 24-May-2012 09:14Add to My Shortlist
JOB SUMMARY: Rare opportunity for a Senior Project Manager/Programme Manager looking to progress into an Associate Director role within a top tier Pharma Company. This role will involve both strategic and scientific leadership for assigned studies and/or have overall Clinical Operations responsibility for a specified compound within the Neuroscience portfolio. May also have responsibility for direct reports, including hiring and... study-related risks are appropriately identified and managed, and ensuring timely and appropriate escalation of study risks to functional head, Clinical sub-team, Project Review meetings and other appropriate forums. Monitoring resource needs for the assigned studies and works with functional management to ensure that these needs are met. * Management of clinical trial costs within the approved budget for the assigned studies * Achievement of relevant Key Performance Indicators for the assigned studies * Contributing innovative thinking and bringing an external market perspective to task execution within and outside area of direct accountability * Acting as an informal mentor and coach to team...
GCP QA Auditor
- Salary:
- To Negotiate
- Location:
- England, Hertfordshire, Essex, Cambridgeshire, Bedfordshire
- Job Type:
- Permanent
- Date Posted:
- 25-May-2012 16:48Add to My Shortlist
As primarily a GCP QA Auditor within the multi-disciplined company QA team you will utilise your expert regulatory knowledge and excellent communication skills to assist with the design and implementation of the audit programme for the clinical development functions, including internal systems, external supplier and essential documentation and investigator site audits. You will also provide support, advice, education and training to other departments involved in clinical trials and pharmacovigilance activities and may become involved with PV, GLP and GMP audits. You will take part in hosting GCP and PV regulatory inspections; assist with the set up and maintenance of procedures within Clinical Development and support the development, maintenance and audit of marketing authorisation application dossiers. This will...
Medical Assessor - Product Safety, Europe
- Salary:
- On Application
- Location:
- Cambridgeshire, Buckinghamshire, Essex, Hertfordshire, London
- Job Type:
- Permanent
- Date Posted:
- 24-May-2012 09:15Add to My Shortlist
Benefits: Corporate Package JOB SUMMARY Excellent opportunity for a UK GMC registered physician looking to join a leading global pharmaceutical company. Based within the EU HQ you will contribute to the provision of a fist class Pharmacovigilance service by undertaking comprehensive medical evaluation of individual case safety reports (both spontaneous and clinical trial) and supporting the General Safety Officers (GSO) in aggregate report production. BACKGROUND Our client is one of the world's leading research-based pharmaceutical companies. Based in Hertfordshire they employee over 11,000 people worldwide. PRIMARY DUTIES * To provide comprehensive medical evaluation of individual adverse event case safety reports (both spontaneous and...
UK- Experienced Senior Clinical Research Associate
- Salary:
- Competitive
- Location:
- Cambridgeshire, Huntingdonshire, Bedfordshire, Hertfordshire, Northamptonshire, Norfolk
- Job Type:
- Permanent
- Date Posted:
- 29-May-2012 00:00Add to My Shortlist
An interesting and varied Lead/Senior Clinical Research Associate vacancy has arisen with our client; a progressive Clinical Research Organisation and regulatory consultancy which specialises in providing practical advice and support to the pharmaceutical industry to move products from early concept and into the clinic. Their main area of focus is in early Phase clinical trials. The Senior CRA will be responsible for monitoring clinical trials sites and will also be the main point of contact for Investigational site staff. They will also be required to act as Lead CRA on multi centre studies and to mentor new and less experienced members of the CRA team. To...
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...
Experienced Clinical Project Manager
- Salary:
- On application
- Location:
- Cambridgeshire, Huntingdonshire, Bedfordshire, Hertfordshire, Northamptonshire, Norfolk
- Job Type:
- Permanent
- Date Posted:
- 25-May-2012 00:00Add to My Shortlist
Experienced Clinical Project Manager (Cambridgeshire, UK) An interesting and varied Clinical Project Manager vacancy has arisen with our client, an expanding Clinical Research Organisation and regulatory consultancy which specialises in providing practical advice and support to the pharmaceutical industry to move products from early concept and into the clinic. Their main area of focus is in early Phase I and Phase II clinical trials. The Project Manager will have primary responsibility for the delivery of Clinical Projects and will be the main point of liaison within the company for the client and associated third-party vendors. The Project Manager will also work with the team to develop and promote the business. This is a permanent, ...
Senior Manager Regulatory Affairs
- Salary:
- On Application
- Location:
- Cambridgeshire, Bedfordshire, Hertfordshire, London, Middlesex
- Job Type:
- Permanent
- Date Posted:
- 26-May-2012 00:00Add to My Shortlist
JOB SUMMARY: Exciting opportunity for an experienced regulatory specialist to join a global organisation offering excellent career progression. You will contributing to clinical development plans, global regulatory strategic plans and providing advice on EU regulatory clinical trial and marketing authorisation requirements to the International Project Teams or Regulatory Sub-team. You will also be responsible for maximising product lifecycle management and licence maintenance for our clients current marketed products BACKGROUND: Our client is one of the world's leading research-based pharmaceutical companies with operations in the U.S., Asia, Europe...
Senior European Medical Information Scientist / Pharmacist
- Salary:
- On Application
- Location:
- Hertfordshire, London, Middlesex
- Job Type:
- Contract/Interim
- Date Posted:
- 24-May-2012 09:17Add to My Shortlist
JOB SUMMARY: Experienced Medical Information Scientist required to a busy department within a global Pharmaceutical organisation. This is a fixed term contract (expires Jan 2013) with the flexibility to work 3 - 4 days/week. Successful applicants will have experience as 2nd line support to European Affiliates, supporting European brand teams and handling first line enquiries from UK HCP's. BACKGROUND: Top... * Responding to AE reports/product complaints and queries and ensuring reports are passed to Pharmacovigilance/Quality Operations as required. Log and maintain appropriate records. * Operate as expert for assigned marketed and development products by: - Identifying and organising clinical information on product, competitors and therapeutic area. - Analysing and evaluating clinical trial results, summarising the key points and advise Marketing teams on their use. -Supporting Marketing and Medical Affairs through thorough copy approval and reference checking for core marketing materials. Checking information content and compliance with ABPI / EFPIA Codes of Practice. - Literature searching and journal scanning for products & competitors...
Contract File Reviewer, Stevenage- UK
- Salary:
- On Application
- Location:
- Stevenage, Hertfordshire, Buckinghamshire, Bedfordshire, Cambridgeshire, Essex, Suffolk
- Job Type:
- Permanent
- Date Posted:
- 25-May-2012 00:00Add to My Shortlist
Novella Clinical is a global, full service CRO with our European Headquarters in Hertfordshire, England. We are committed to providing a superior service to our global clients, and as such we are seeking to hire the best Clinical Research Professionals in the industry. We are currently looking for an experienced Document Control Specialist to work in our offices based in... are also proud of being one of the very few global CROs to work to the high standards of ISO accreditation. Principal responsibilities will include: * Responsible for coordinating with other departments to ensure all electronic and paper storage needs are prepared and maintained * Maintain contact with project managers, clinical trial managers and CRAs to obtain the necessary documentation throughout the trial, for document quality control * Collaborate in the development, maintenance, and archive of study-related web portals * Collaborate in the development, maintenance, and archive of Novella's electronic document management system, as well as, ensure accuracy and consistency * Assist...
Manager Statistical Programming
- Salary:
- Competitive
- Location:
- Hertfordshire, Stevenage, Letchworth, Hitchin, Welwyn Garden City, St Albans, Hemel Hempstead, Watford, Hertford, Ware, Bishop's Stortford
- Job Type:
- Contract/Temp
- Date Posted:
- 25-May-2012 11:09Add to My Shortlist
Manager Statistical Programming - Location: Hertfordshire CK Clinical are recruiting for a Manager Statistical Programming to join a global pharmaceutical company at their site based in Hertfordshire on a 6 months contract. As Manager Statistical Programming the main purpose of your role will be to: - Support the Biostatistics team by supporting the computing environment - Contribute to the overall... - Writing and Executing systems and macro testing (IQ/OQ/UAT), and delivering training. As Manager Statistical Programming, you will have the following qualifications, skills and experience: - Bachelor's degree in Statistics, Computer Science, Mathematics, or a related science discipline preferred (Masters degree preferred) - Experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment - Some management experience in a pharmaceutical/CRO programming environment or demonstrated significant leadership of SAS programming activities in a clinical pharmaceutical/CRO environment - Validation and Systems Development Life Cycle - Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office. Proven experience with Unix and Windows operating...
Senior Medical Advisor Analgesics
- Salary:
- On Application
- Location:
- Cambridgeshire, Norfolk, Suffolk, Bedfordshire, Essex, Hertfordshire, London
- Job Type:
- Permanent
- Date Posted:
- 26-May-2012 00:00Add to My Shortlist
Benefits: + Car allowance + bonus + health + Life insurance + support for Higher Medical Training in Pharmaceutical Medicine JOB SUMMARY: Excellent opportunity for an experienced Medical Advisor to step up to a senior role with line management responsibility in this specialist independent pharmaceutical company. Based in state of the art offices in Cambridge. BACKGROUND Our client is an...
Study Start Up- UK
- Salary:
- On application
- Location:
- Stevenage, Hertfordshire, Buckinghamshire, Bedfordshire, Cambridgeshire, Essex, Suffolk
- Job Type:
- Permanent
- Date Posted:
- 25-May-2012 00:00Add to My Shortlist
Novella Clinical is a global, full service CRO with our European Headquarters in Hertfordshire, England. We are committed to providing a superior service to our global clients, and as such we are seeking to hire the best Study Start Up professionals in the industry. We are currently looking for an experienced Study Start Up Lead to work in offices based... Strong written and verbal communication skills to express complex ideas to study personnel, internal and sponsor team members. * Excellent organizational and interpersonal skills. * Positive attitude and ability to interact with all levels of staff to coordinate and execute study activities. * Ability to manage multiple priorities within various clinical trials. * Working knowledge of current ICH GCP guidelines and applicable regulations. * Ability to reason independently, assess and recommend specific solutions in clinical settings, and mentor entry level start up staff. If you are interested in Novella Clinical and would like to be a part of our team, please submit...