Clinical Document Coordinator
- Employer
- Thornshaw Recruitment
- Location
- Dublin (County), Leinster (IE)
- Salary
- Neg
- Start date
- 7 Jun 2023
- Closing date
- 5 Jul 2023
View more
- Discipline
- Clinical Research, Clinical Administrator
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Job Details
Clinical Document Coordinator
Collaborating with my client, a clinical stage medical devices company on a new vacancy for a Clinical Document Coordinator. This is a new role and a fantastic opportunity to join a young growing company.
Reporting to the Clinical Project Manager, your role will support the execution of clinical development plans with the primary responsibility to develop new and evolve existing clinical documents used in the execution of clinical trials.
Key Responsibilities:
- Generate clinical study documents required to support clinical activities.
- Lead evolution of documents as clinical studies progress, including cross referencing to supporting documents to ensure connectivity and continuity throughout documents supporting clinical execution.
- Support with responses to competent authorities and ethics committee and/or review boards.
- Assist in maintaining study management documentation used to support strategic discussions.
- Other duties - support the development of the technical documents and standard operating procedures in support of clinical development plan, organising key publications and performing literature searches as required.
- Support the running of internal team and external meetings as needed by the project and be an integral part of the Clinical Development team.
Engage with the company QMS to ensure delivery of the overall quality strategy & support the achievement of the business quality objectives.
Qualifications & Experience
- Bachelor’s Science Degree, or equivalent Clinical trial experience for a minimum of 1 years. Exceptional attention to detail. Excellent communicator with experience developing relationships with stakeholders to understand their requirements. Well organised with experience working to deadlines. Ability to proactively identify issues and make recommendations. Technically proficient with PowerPoint, Excel, and Word.
For further details contact Tina at +353 1 2784701 or 087 6811990 or email to tdunne@thornshaw.com. Thornshaw Scientific is a division of the CPL Group. www.thornshaw.com
Company
Thornshaw Scientific Recruitment was first established in 1999 and since then has become a leader in Scientific recruitment. In 2005 we partnered with Cpl Resources, one of Europe’s most successful recruitment companies.
Our wealth of experience in specialised recruitment allows us to offer the right solution to each employer, whatever their recruitment requirements.
Over the years we have developed strong relationships with our clients in the market and we pride ourselves on our repeat business from clients.
Our Industries
We are a global provider and have been providing a reputable recruitment service to the Biotech, Pharmaceutical, Clinical Research, Medical Device, Engineering and Healthcare industries for over 20 years.
Our Specialities
Clinical Research, Regulatory Affairs, Quality Assurance, Medical Affairs, Pharmacovigilance, Biostatistics, QC, Validation.
Our Mission
For further details on our services contact Tina at +353 1 2784701 or email tdunne@thornshaw.com
- Website
- http://www.thornshaw.com/
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