Regulatory Clinical Trials Submission Manager

ProPharma Group is the leading global, independent, single-source provider of regulatory, clinical, and compliance services serving pharmaceutical, biotechnology, and medical device companies. Our team of experts brings a comprehensive portfolio of regulatory sciences, clinical research solutions, life science consulting, R&D technology, pharmacovigilance,...

ProPharma Group is the leading global, independent, single-source provider of regulatory, clinical, and compliance services serving pharmaceutical, biotechnology, and medical device companies. Our team of experts brings a comprehensive portfolio of regulatory sciences, clinical research solutions, life science consulting, R&D technology, pharmacovigilance,...

Job Details: Regulatory Submissions, Manager Full details of the job. Vacancy Name Vacancy Name Regulatory Submissions, Manager Vacancy No Vacancy No VN188 Employment Type Employment Type Permanent Location of role Location of role Abingdon About the Company About the Company Immunocore (NASDAQ: IMCR) is a pioneering, commercial-stage T cell...

We are seeking for an enthusiastic experienced Clinical Trials Manager to join our Clinical and Application Research department. You will be responsible for all aspects of clinical trial management. Duties will include designing plus authoring trial documentation and regulatory submissions, plus monitoring the progress and performance of multiple trials from...

Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Anchored in our company’s scientific heritage, our dedicated therapeutic focus on cardiovascular,...

Who we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Anchored in our company’s scientific heritage, our dedicated therapeutic focus on...

CTA Submission Manager - Homebased in UK/ Europe ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations. With our patients at the center of...

Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality.Anchored in our company’s scientific heritage, our dedicated therapeutic focus on cardiovascular,...

Who we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Anchored in our company’s scientific heritage, our dedicated therapeutic focus on...

Who we are: Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications - from discovery to reality. Anchored in our company’s scientific heritage, our dedicated therapeutic focus on...

Regulatory Submissions, Manager Vacancy Name Regulatory Submissions, Manager Employment Type Permanent IMCR) is a pioneering, commercial-stage T cell receptor biotechnology company whose purpose is to develop and commercialize a new generation of transformative medicines which address unmet patient needs in oncology, infectious diseases and autoimmune...

Precision for Medicine (CRO) are recruiting a Regulatory Manager to join our team, candidates can be based in the following countries: UK, Spain, Hungary, Slovakia, Serbia, Romania or Poland. The Regulatory Manager (RM) provides regulatory strategy and development guidance for optimal conduct of clinical trials, regulatory agency meetings, orphan...

IQVIA’s cFSP (sponsor-dedicated) team are seeking a Clinical Trial Manager to join us on our mission to drive healthcare forward. The Clinical Trial Manager will partner with the Clinical Trial Assistants, Clinical Research Associates, Central Trial Managers and Global Trial Managers to ensure overall study delivery at country level. RESPONSIBILITIES ...

Who we are: Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality.Anchored in our company’s scientific heritage, our dedicated therapeutic focus on...

Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Anchored in our company’s scientific heritage, our dedicated therapeutic focus on cardiovascular,...

We are currently looking for Regulatory Affairs Professionals experienced in Clinical Trail Applications (CTAs) under EU-CTR directive . You can join us or our client dedicated projects and act as a Regul atory Affairs Consultant or Regulatory Affairs Senior Associate. This role can be based in either UK or UE (home/office based). In this role you...

Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Anchored in our company’s scientific heritage, our dedicated therapeutic focus on cardiovascular,...

IQVIA’s cFSP (sponsor-dedicated) team are seeking a Clinical Trial Manager to join us on our mission to drive healthcare forward. The Clinical Trial Manager will partner with the Clinical Trial Assistants, Clinical Research Associates, Central Trial Managers and Global Trial Managers to ensure overall study delivery at country level. Partner with...

Gabriel Roberts is working with a startup CRO who are looking for their first CTA to join their small but passionate team!My client has very strong core values which results to a great work environment and very happy staff!This role is working in remotely in the UK. This is a unique opportunity to grow with a company and be there for all their successes!Key...

Gabriel Roberts is working with a startup CRO who are looking for their first CTA to join their small but passionate team! My client has very strong core values which results to a great work environment and very happy staff! This role is working in remotely in the UK. This is a unique opportunity to grow with a company and be there for all their successes!...