- Regulatory Affairs Consultant-Innovative Medical Devices-Basel
Register and work with innovative medical devices in this new position within regulatory affairs. Our client, based in Basel are looking for a regulatory affairs consultant to join their team permanently to work on international projects across class I through to class III medical devices. This is a great opportunity for a regulatory affairs professional to develop their skills across a range of devices on a global scale.
- Senior Medical Writer
Senior Medical Writer (Contract) –Home-basedAn exciting opportunity to join a fast paced and dynamic team in one of the leading CROs in the world. The Senior Medical Writer researches, creates and edits all documents relating to clinical trials. You will be the primary contact for medical writing projects, setting timelines, providing leadership and running training to support more junior writing staff. ...
- Medical Devices Statistician
Medical Device Statistician The opportunity is with one of the world's top global medical device company as a senior statistician, working on observational studies on the worlds ground breaking studies in diabetics diagnostics with a team of in house research team. The role is permanent, with a view for candidates across the EU and UK
- Sr Project Leader Analytical Development APIs (m/f)
Sr Project Leader Analytical Development APIs (m/f)office-based in BaselRole:* As Sr Project Leader Analytical Development APIs you will be responsible to support the analytical development of APIs done internally, as well as externally (such as CMOs). ...
- Regulatory Consultant - Medical Devices - Freelance
Freelance Regulatory Consultant - Medical Devices
- Clinical Research Physician – 6 month contract - £900 a day – London
We are a Global Pharmaceutical looking for a CNS specialised Physician to act as a Medical Monitor for several high profile trials and have input into clinical strategy decisions.
- Medical Monitor Oncology – 6 month contract – Global Top 10 Pharma - Hertfordshire
This Global Top 10 Pharmaceutical are looking for a highly Oncology specialised Physician to act as a trial level monitor for Phase IIb – Phase III Global Oncology studies.
- Clinical Study / Trial Manager – Global Pharma – 6 Months - £400~ per day
We are looking for a Clinical Study Manager with experience in Oncology for a 6 month contract with probable extensions, the position is office based in Buckinghamshire. The successful candidate will be working in rapidly growing company in one of their strongest teams, focusing on Phase II and III studies. This is an exciting opportunity for anyone wanting to expand their study management experience in a globally successful and growing company.
- Associate Clinical Trial / Study Manager – 12 Month Contract – South East England - £300+ per day
We are recruiting for an Associate Clinical Trial/Study Manager for a 12 month contract, office based in South East England. The therapy area in Ophthalmology, a strong pipeline in this company and the role will be a supporting position for the Study Manager. Phase III Global Study experience is required. If this sounds of interest, do not hesitate to get in touch by email@example.com.
- CRA II - Single Sponsor - Reduced Travel - ONCOLOGY
JOB TITLE CRA II – Reduced Travel – Leeds / Yorkshire JOB SUMMARYThis leading speciality drug development organisation with an international presence is seeking an experienced CRA who has been working on complex studies, across a range of therapeutic areas, including but not limited to Oncology, Cardiovascular, Diabetes and CNS. This is an excellent opportunity to work directly with a Sponsor on Oncology studies in Phase I-III. ...