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Search Results for Clinical Research Associate
Job Title. | Location | Salary | Actions |
Clinical Affairs ManagerClinical Affairs Manager Our client, a medical device organisation, are currently recruiting for Clinical Affairs Manager to join their team on a permanent basis. As Clinical Affairs Manager you will, lead and participate in clinical project teams as part of the company’s clinical programs. The clinical programs include first in human, pilot, pivotal and post-launch studies. You will manage multiple operational studies, provide oversight throughout the development, implementation and conduct of clinical studies globally, develop study plans an...Location: Galway, |
Galway | Not Disclosed | |
Associate Director Clinical Trial CapabilitiesAssociate Director Clinical Trial Capabilities Our client, a global pharmaceutical organisation are currently recruiting an Associate Director to join their Clinical Trials Capabilities team on a permanent basis. As Associate Director you will lead the clinical trial capabilities in support of clinical development. This is an exciting opportunity which will allow you to provide leadership, direction and technical support to the Clinical Trial Capabilities Teams focusing on results and driving efficiency to achieve goals and objectives Responsibilities: Lead and co...Location: Cork, |
Cork | Not Disclosed |
Clinical Research Associate Career Profile
Clinical Research Associate
The Clinical Research Associate is tasked with monitoring clinical trials sites in order to ensure that studies are carried in accordance with the study protocol, the company standard operating procedures (SOP), applicable regulations and the principles of ICH - GCP (International Conference on Harmonisation - Good Clinical Practice).
Key Responsibilities
- Identification of key investigators
- Assistance in the preparation of regulatory submissions
- Design patient information sheets and consent forms
- Coordinate document translation and verification
- Ensure timely submission of protocol/consent documents/safety reports for Ethics/IRB approval according to local requirements
- Pre-study and initiation visits
- Conduct regular monitoring visits in accordance with the trial site monitoring SOP
- Maintain all files and documentation pertaining to studies
- Motivate investigators in order to achieve recruitment targets
- Complete accurate study status reports.
- Ensure the correct storage of drugs and the diligent account of all drugs in accordance with SOPs
- Keep the project manager regularly informed
- Process case record forms to the required quality standards and timelines
- Ensure the satisfactory close-out of investigator sites
- Ensure correct archiving of files on completion of a study
- Co-operate with QA personnel in the conduct of QA audits
- Participate in feasibility studies for new proposals
- Maintain patient confidentiality
Qualifications / Experience Required
- Degree in Life Sciences or Equivalent
- Ability and willingness to travel at least 50% of the time, both international and local
- Ability to review and evaluate clinical data
- Computer literacy desirable
- Foreign language skills desirable
- Current full driving license essential
- Good oral and written communication skills
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Pharmaceutical | Tel:+353 1 685 4545 | Fax: +353 (0)1 443 05 24 | Email: [email protected] | Copyright © 2012 Life Science Recruitment Ltd
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Pharmaceutical | Tel:+353 1 685 4545 | Fax: +353 (0)1 443 05 24 | Email: [email protected] | Copyright © 2012 Life Science Recruitment Ltd
This site uses cookies. For more information on our cookie policy visit Privacy Policy | Terms of Use
Registered as a private limited company. No: 445328 |
Web Design / SEO by WebScience | Valid XHTML - CSS