REGULATORY CLINICAL STRATEGY SUBMISSIONS jobs in UNITED KINGDOM, United Kingdom

the submission strategy for clinical trials planned globally are in accordance with the overarching global regulatory... overarching global regulatory strategy considering regional specific requirements. Represent area regulatory in clinical trial...

SRG

Reference Number: JO-2404-532643 Regulatory Strategy and Submissions Manager Rate: Negotiable Job Type: Contract..., amendments, and strategies Provide leadership and expertise in regulatory and submissions-related aspects of clinical trials...

Clinical Professionals

, and strategies Provide leadership and expertise in regulatory and submissions-related aspects of clinical trials... several EU CTR submissions. As a Regulatory Affairs Professional, you will assume a crucial role in providing leadership...

Cpl Group

and compliant submissions and approvals. Advise senior management on regulatory and clinical strategy pathways and options... with regulatory registration strategy. Support the build of global clinical development strategy based on correct interpretation...

Ortolan Group

Job Description Join our team as a Clinical Quality Operations Lead - Inspection Strategy and be at the forefront... and guidance will ensure the smooth management, training, and support of regulatory Health Authority inspections, solidifying...

MSD

publication strategy and conference submissions. Responding to questions from regulatory authorities to ensure adherence to the... appropriate regulation. Work closely with other collaborators and relevant clinical strategy leads to support regulatory related...

Smith & Nephew

related to clinical trial submissions managed by other stakeholders such as IB, Protocols. Ensuring the approved company...Reference Number: JO-2404-533971 Regulatory Coordinator Rate: Negotiable Job Type: Contract Location: Reading...

Clinical Professionals

you will be responsible for building strategy, determining regulatory requirements and managing product license registrations with global... and compiling regulatory documentation, coordinating and executing regulatory submissions in compliance with ISO13485, IVD 2017/746...

Clinical Professionals

regulatory strategy, determining applicable regulatory requirements, proposing solutions to comply with regulatory requirements...Reference Number: JO-2403-531737 Senior Regulatory Associate Rate: Negotiable Job Type: Permanent Location...

Clinical Professionals

regulatory submissions, driving regulatory strategy, new registrations, and variations applications for a range of different... products including submitting submissions through National MRP and DCP. · Drive/support European regulatory strategies...

Clinical Professionals

Managers and Regulatory Director you will be responsible for generating regulatory submissions to target markets throughout... of regulatory applications (generally DCP, MRP,CP or national submissions) including responses to requests for further information...

Clinical Professionals

for submission in the relevant countries. Manage strategy and execution for all regulatory CMC submissions (e.g. late stage clinical... regional issues impacting global regulatory strategy for proposed CMC filings are considered and risks identified...

CK Group

for submission in the relevant countries. Manage strategy and execution for all regulatory CMC submissions (e.g. late stage clinical... regional issues impacting global regulatory strategy for proposed CMC filings are considered and risks identified...

CK Group

Clinical Trial Strategy & Submissions Team as required. § Comply with the company's policies and procedures. Skills... CTA experience in global clinical trial submissions to regulatory agencies. § Experience working effectively...

SRG

and manage regulatory submissions (e.g. clinical trial and marketing applications) for products within the client's portfolio... and/or support staff. Responsible for: Advising the Global Regulatory Team on regional considerations in developing strategy...

Achieva Group

embedded role ICON’s Regulatory Strategy group, you will lead or contribute to the development and execution of the drug... and making regulatory submissions via CTIS. You will be supporting the EU regulatory team with planning and executing regulatory...

ICON

and manage regulatory submissions (e.g. clinical trial and marketing applications) in compliance with global filing plans... interactions consistent with the Global Regulatory strategy- including contingency regulatory planning/risk assessment. Plan...

CK Group