They are on the search for a new Associate Director to manage the end-to-end clinical trial process. Extensive experience in Clinical Research within a Pharmaceutical/Biotechnology or CRO industry environment, as well as a significant time of in-depth clinical trial management and team management...
Provide leadership and where required, management of Project Data Managers and other staff, in addition to leadership and management of projects and clinical trial data from design of the study through to final delivery of clinical datasets. You will act as the primary Data Management Lead for as...
The IVD Clinical Research Associate will design, plan, coordinate, and conduct all activities involved in initiating, monitoring, and completing clinical research studies for in vitro diagnostics. Ensuring studies are conducted and documented in accordance with the study protocol, standard operat...
Senior Clinical Research Associate. Unique opportunity here to join a small CRO, scaling up their clinical operations team, led by an industry leader that has previously found success in establishing another leading global CRO. You'll be working directly with Senior leadership within Clinical Ope...
The Associate Project Manager will support the Project Management Team and contribute to the successful delivery of IXICO’s clinical trials, research studies and collaborations under the guidance and supervision of more senior team members. Assist Project Manager(s) with defined project tasks on ...
Role: Clinical Trial Assistant (CTA / Associate CPM). They have a vacancy open for a Clinical Trial Assistant (CTA) to join their team and they can take someone on immediately. Provides input into clinical study protocols, clinical study reports, and other clinical documents as appropriate on ass...
Minimum of 4 years' experience clinical study management/clinical project management as a study manager/clinical project manager. ICON plc is looking for a Global Clinical Project Manager (CPM) to join one of the brightest minds in the industry to transform clinical research. In the role of a Glo...
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Previous experience managing clinical research trials/projects (preferably 3 years). To manage the life cycle, from start up to close out conduct of post-authorisation studies and interventional clinical trials in accordance with protocols, both local and international regulations, GxP guidelines...
Clinical Project Manager / Senior Clinical Project Manager. As a Clinical Project Manager, you will become part of a team working for and reporting to the Head of Clinical. You will be expected to take responsibility for overseeing clinical trial administrators and other project team. Oversees al...
As the new Clinical Research Associate, you will be responsible for overseeing trial sites, managing trial data, ensuring compliance with regulatory requirements and maintaining the integrity of study protocols. We are looking for an experienced Clinical Research professional with proven experien...
The CRA is responsible for adhering to the policies of the quality system and achieving quality objectives through daily actions. Up to 2 years of experience in CRA IVD role preferred but not required. ...
Senior Clinical Project Manager. If you have a clinical background and are interested in joining an exciting international organisation then this could be the role for you!. They are a well funded organisation that is continuously growing their Clinical Operations team. Plan, deliver and manage c...
- Role: Clinical Trial Assistant (CTA / Associate CPM) * Location: Hybrid (4 days remote and 1 day per week in London) * Company: Small Biopharmaceutical Company * Salary: £35,000 - £42,000 ...
... Associate Clinical Project Manager on a permanent full-time capacity. Purpose of the Role: The ... trial. * Experience of working in an environment governed by SOPs and working within those SOPs
... to trial. The firm is recognised nationally for its outstanding client care and high-quality ... Clinical Negligence Solicitor / Associate * Experience of working on a Multi Track Litigated ...
Business Development Associate Location: Hemel Hempstead Working Hours: Monday - Friday, 9am - 5 ... clinical trial to help make fertility treatment available worldwide. · Hosted international ...
Blackfield Associates are currently supporting a growing and bespoke management consultancy ... Providing strategic recommendations on a global clinical trial design to enable HTA and ...
Respond to information requests to HCPs as requested; this may include clinical trial discussions, pipeline data and other appropriate forms of scientific engagement * Co-ordinate and utilise ...
To source, negotiate and broker all care placements, extra care and domiciliary care packages for service users with more complex needs within and outside the established commissioning and procurement frameworks.To assists as appropriate with the quality assurance and monitoring for all direct pa...
South/Central London based Local Authority.Multi-agency Violence and Exploitation (MAVE) and Multi-agency Child Exploitation (MACE) Panel Coordinator.To coordinate and administrate the Lambeth Multiagency Violence and Exploitation (MAVE) and the Lambeth Multiagency Child Exploitation (MACE) Panel...
Months contract with a Local Authority.We are seeking someone to join the Commissioning Team as the Mental Health Commissioner responsible for the review of mental health service provision across Slough.This post will lead in the strategic review of mental health provision as well as designing an...
Permanent Role with a South London based Local Authority.A senior social worker within a dedicated court team.They will need to be able to manage cases within court proceedings from initial hearing to final and then to adoption if needed.They will need to produce a good standard of report writing...