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Clinical Research - Clinical Trial Regulatory Affairs Consultant Jobs - Strathclyde

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Clinical Research - Clinical Trial Regulatory Affairs Consultant Jobs - Strathclyde (Job Ref: WR/JOBS/24883-11368)

Job Ref : WR/JOBS/24883-11368
Discipline : Clinical Research/Regulatory Affairs
Contract : Permanent
Salary :  Competitive

Vacancy Location
: Strathclyde View Map


Job Description :

Job Summary

Regulatory Affairs – Clinical Trial Regulatory Affairs Consultant Job – Glasgow or Edinburgh:

UK: Salary up to £30k

Flame Pharma is working alongside a global clinical research organisation providing the full range of early– to late–stage clinical development services for the world’s bio pharmaceutical industry. As the Clinical Trial Regulatory Affairs Consultant you will be responsible for providing advice and assistance to clients and other associates on clinical trial requirements. You will be working closely with Senior Clinical Trial Regulatory Consultants and Associate Directors and you will already posses an excellent understanding of the clinical trial application process and have strong negotiating skills.

The Role

Reporting to the Senior Clinical Trial Regulatory Affairs Consultant you will be responsible for performance on major projects & prepare Regulatory Submissions with guidance from Senior Clinical Trial Regulatory Consultants or Associate Directors. This role comes with the Responsibility for completion of assignments on time to cost and quality requirements, with a proactive approach to assignments and you will be developed in an area of special skill and provides an in-house resource. You will be required to Arrange, participate and report on client meetings and regulatory authorities, with managerial supervision.

The Person

You will be a regulatory affairs professional with direct clinical trial regulatory experience, Sound and current regulatory knowledge, with an understanding of the critical path of pharmaceutical product development and a full knowledge of clinical trial application process, with the ability to interact effectively with both clients and employees.

Key Words

Regulatory Affairs, Senior Regulatory Affairs Consultant, Pharmacovigilance, Drug Safety, Director, Manager, Management, Clinical Research, Clinical Trials, Medical, Clinical, CRO, Study Management, Clinical Management, Pharmaceutical, Career, Research, Hertfordshire, Job, Recruitment














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