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Job Title
- CRA 232
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Regulatory Affairs Director - Innovative Medical Device Organisation - Netherlands
An excellent opportunity has arisen for a Regulatory Affairs Director (Head of) to join a Medical Device organisation that have recently transition...
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Genetics – Director – Gene Therapy Ophthalmology
We have an exciting opportunity available as a Director of Genetics at a cutting edge Biotechnology company based in South East England. This is a ...
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Regulatory Consultant
12 month contract for regulatory consultant in MA renewals/variations/applications and maintenance with opportunity to work from home 2 days a week
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Director – Clinical Development Sciences – Gene Therapy
We have an exciting opportunity available as a Director of Clinical Sciences at a clinical-stage Gene Therapy Biotechnology company specializing in...
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Clinical Systems Product Manager
Clinical Systems Product Manager - Anywhere, USOffice based or Remote basedWho We Are Synteract is a global full-service contract research organizatio
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Clinical Trial Manager
Clinical Trials Manager - Anywhere, USOffice-based in Morrisville, NC or Carlsbad, CA; Remote anywhere in the US Who We Are Synteract is a global full
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SWIFT Alliance Administrator
JOB TITLESWIFT Alliance Administrator - 6+ month contractTHE COMPANYOne of the top Biopharms companies in the world. The organisation is seeking a tal
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Manager, Data Management
The Manager is responsible for the oversight of a team or group. This includes ensuring successfulperformance and delivery of his/her direct report's
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Regulatory Affairs Associate
We are currently looking for an Associate who will have the following responsibilities: Responsible for the publishing, and quality control of Regula
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Principal Regulatory Affairs Consultant(Non-Clinical SME)(UK/EMEA)
We are currently seeking an EU Non-Clinical SME, aligned with the following profile:* The role can be office or home based in one of our EMEA location
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Project Leader, Real World Evidence
PAREXEL strives to be the premier provider to the biopharmaceutical and medical device industries for the development and commercialization of new med
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Research Associate LVN
Key AccountabilitiesIncluding but not limited to the following and other duties as may be assigned: Has detailed knowledge of the study protocols, lab
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Regulatory Affairs Associate
Main accountabilities: Responsible for the publishing, and quality control of Regulatory submissions (eCTD core package creation; eCTD baseline; eCTD
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Payment Coordinator
Job SummaryThis is a great opportunity for an experienced CTA/SSU/Contract Specialist with experience in Site Payments to join an international team w
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CRA
Job SummaryThis is an exciting opportunity to become part of a dynamic and successful international Biotechnology organization. The company is ranked
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Senior Site Manager
Job SummaryDocs has partnered with one of the world's leading pharma companies on a global study management initiatives that has created exciting oppo
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SITE MANAGER
Job SummaryThis is a great opportunity for a Clinical Research Associate with experience in Inmunology looking for a new challenge! You will be part o
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SR SITE MANAGER
Job SummaryThis is a great opportunity for a Clinical Research Associate with experience in Hematology looking for a new challenge! You will be part o
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CLINICAL TRIAL ASSISTANT - ATV
Job SummaryDocs has partnered with one of the world's leading pharma companies on a global study management initiatives that has created exciting oppo
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CRA II / SR CRA
Job SummaryThis is a great job opportunity for an experienced CRA to work on behalf of an international Biotech Company, full time, permanent and home
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