- Clinical Operations Manager / COM - Sweden, Stockholm, Solna - (SSU / Study Start Up / Submissions)
As a Clinical Operations Manager at ClinTec you'll have a significant impact on how the sponsor can deliver country-specific trial commitments and objectives, especially during study start-up.
Key Experience (Study Start Up / SSU, Submissions, Ethics, Regulatory)
By working for ClinTec you can further your career in a dynamic, fast-paced environment and you can be assured of rewarding benefits.
- (Senior) Project Manager, Study Start Up (home based, flexible location in Europe)
We are currently seeing a big growth in our study start-up team and are looking for a number of new colleagues all over Europe. This is a very exciting time for Covance and for the study start-up team. We are now looking for a (Senior) Project Manager Study Start-up. In this role you will have a great opportunity to progress in your career and develop. The role is home based in a variety of locations in Europe.
- Regulatory Submissions Manager
Medpace is seeking a Regulatory Submission Manager for our office in Sao Paolo.
- Regulatory Affairs Project Manager \ Regulatory Consultant - Freelance
Regulatory Affairs Project Manager \ Regulatory Consultant - Freelance : West London or home based. Do you want to be part of an innovative and scientifically-driven contract research organisations?
- Study Start-Up Specialist II Germany
As "Study Start-up Specialist II" you will act as 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 "Study Start Up Specialist" may be assigned to more than one Project. At times you may also have the opportunity to be involved with startup activities for multiple countries.
- Clinical Study Manager
Clinical Study Manager. Warwickshire.Medical Devices. Our client is a well-funded start-up organisation who have developed an innovating advanced portable haemodialysis product designed for use in the home and clinic
- Freelance SSU - Homebased
Freelance Study Start-Up Specialist - 1FTE - Office/Home Based - BelgiumTired of the travelling of a CRA? I have a homebased position in Belgium offering limited travel and the opportunity to be in a great working team.I am partnering with a global CRO who are searching for a study start up associate to join there team. The initial contract it for 6-12 months, but from previous experience it will be extended beyond this.
- 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.
- Clinical Project Manager (Junior/Senior)
Clinical Project Manager (Junior/Senior)Global top 10 CRO providing clinical development services (Phase I to IV) for the pharma industry worldwide.LOCATIONSpain (Madrid, Barcelona)ROLE* Manage multi-functional project teams to ensure proper use of study tools/materials and compliance with standard processes.* Create management plans, team assignments and accountabilities, oversight of database maintenance.* Manage communication and reporting schedules with Sponsor. ...
- Regulatory Affairs Project Manager
Regulatory Affairs Project Manager
Salary: £45,000 - £55,000 + great benefits
Are you a Regulatory Affairs candidate with Ethics Committee and Competent Health authorities' submission experience?