- Clinical Study-Start up Specialist, Study Start-up, In-house CRA, Regulatory submissions Co-ordinator
Clinical Study-Start up Specialist, Study Start-up, In-house CRA, Regulatory submissions Co-ordinator, Regulatory associate, CTA, Clinical Trial Associate – London/ M4 Corridor / Home based. We are currently recruiting for a highly recognised CRO that are growing their study start-up team as a core function. Please contact Zoe Benningfield on 07896 693960 or email email@example.com
- Manager, SSU & Regulatory -Italy
Do you want to be a part of a global top 10 CRO? INC Research is a full-service clinical research organization, providing the full range of Phase I to IV clinical development services for the world’s pharmaceutical, biotech and medical device industries. We do this across six continents. We believe that therapeutic and operational experience forms the foundation for taking medicines successfully through clinical development.
- (Senior) Project Managers of Site Activation Services (Study Start Up) with flexible location in Europe
We are currently seeking a proactive, driven Project Managers/ Senior Project Managers to join our expanding Global Site Services team (flexible location in Europe).
- Clinical Study-Start up Specialist, Study Start-up, Clinical Contracts Associate – Circa £40,000 – HOMEBASED
Clinical Study-Start up Specialist, Study Start-up, Clinical Contracts Associate – FEASIBILITY FOCUSED –excellent opportunity to move into a CRA role if desired – Circa £40,000 – HOME BASED. We are currently recruiting for a Top 5 CRO that are growing their study start-up team as a core function. Please contact Zoe Benningfield on 07896 693960 or email firstname.lastname@example.org
- Senior Manager, Study Start Up - Site Activation (office based in Maidenhead or home based UK wide).
At the moment we are looking for a Senior Manager, Site Activation in UK (office based in Maidenhead or home based).
- Regulatory Submissions Manager
Medpace is seeking a Regulatory Submission Manager for our office in Sao Paolo.
- Manager, Site Services
Chiltern is a leading mid-sized CRO that listens to client needs in order to customize solutions for the Biopharma industry. With a 32 year history, Chiltern delivers globally with therapeutic expertise in oncology, respiratory, anti-infectives / vaccines, ophthalmology and dermatology. Chiltern’s 3,700 engaged professionals work across 47 countries to deliver flexible, responsive solutions that are “Designed Around You”.
- Freelance (Senior) Study Start-Up Specialist Germany
inVentiv Health Clinical is a leading provider of global drug development services to pharmaceutical, biotechnology, generic drug, and medical device companies. With 6,500 passionate employees supporting clients in more than 70 countries, inVentiv Health Clinical works to accelerate high quality drug development programs of all sizes around the world.
- In House CRA (study start up)
Chiltern Source acts in a similar way to that of a staffing solutions provider. Chiltern Source supplies high quality and experienced clinical professionals to the pharmaceutical industry, we currently have over 400 staff working with our clients globally. The department is currently seeking a UK Clinical Trials SET UP SPECIALIST. You would be employed by Chiltern Source and seconded out to a top ten pharma company on a rolling yearly contract.
- Start-Up Specialist II, Slovakia (contractor)
inVentiv Health -Transforming Promising Ideas into Commercial RealityJob Title: Start-Up Specialist II, Slovakia (contractor)Primary Function:A local specialist regarding regulatory Institutional Review Board (IRB) and Ethics Committee (ED) processes and documentation requirements for the start-up and conduct of clinical trials according to Good Clinical Practice and local regulations. A Global Study Start Up Specialist may be assigned to more than one project. ...