Research Physician x 3

"Research Physician" and Safety, "Clinical Trial", Phase I, "Phase II", "Study Team". My client, a Leading CRO is looking for 3 x Research Physicians to help with upcoming projects.

The successful candidates will be responsible for performing the following duties;

- Serve as an investigator during the clinical part of the Phase I-II trials performed at the unit. Ensure the medical safety and well being of patients/volunteers during trials. Review and assess the scientific value and potential volunteer safety issues of study protocols.
- Assist with relevant input to the conduct and execution of assigned studies as warranted during the bid process, Site initiation visit, during the actual conduct of the trial and during safety conference calls.
- Assist study team to address the necessary precautions concerning volunteer/patient safety and well being.
- Assist the study team to assess study specific resource requirements and to obtain the necessary training when appropriate.
- Review, prepare and/or submit study specific applications to the Ethics Committee per established study specific time lines. When applicable provide summary for the Ethics committee.
- Liaison with the Phase 1 Global Safety review committee for first-in-human studies as per my client's procedures.
- May review and approve study specific CRF and other documents as assigned.
- Perform studies according to the protocol.
- Complete Protocol specific exams, procedures, and assessments of labs, ECGs, PFTs, etc. per protocol/specifications.
- Assist Physician team to select protocol qualified volunteers per study specific inclusion and exclusion criteria. Focus on volunteer safety.
- Ensure the accuracy, completeness, legibility and timeliness of CRF recorded data, especially AE data.
- Inform the sponsor of adverse events and Serious Adverse Events per established protocol and procedures and to arrange for appropriate follow up of treatment.
- Attend Project Meetings with the sponsor and other team members as warranted.
- Co-operate with the study monitor and reserve sufficient time for questions during monitoring.
- Make sure that Clinical Trials Reports prepared are ICH-GCP compliant and meet the requirements of the sponsor.
- May attend relevant scientific meetings and conferences in order to represent Phase I.
- May serve as PI if approved by Supervisor, Sponsor, and Ethics Committee
- Maintain, in conjunction with Phase I Quality Assurance, the necessary quality standards related to my client's Transnational requirements, SOP's policies and guidelines.
- Attend (as assigned) client specific scientific meetings about proposed forthcoming studies.

If you are interested i hearing more on this opportunity then please call Phil Rose or email your CV

Allegis Group Limited and Aston Carter Limited operate Employment Businesses and Agencies and are companies within the Allegis Group Inc. group of companies, the fourth largest staffing company in the world, (collectively referred to as the "Allegis Group"). TEKsystems and Aerotek are divisions of Allegis Group Limited. Applicant data will be treated in accordance with the Allegis Group's Privacy Notice. By submitting personal data to any company or division within the Allegis Group, the applicant is providing explicit consent to the use of such data by the Allegis Group and to the transfer of such data to and from the Allegis Group companies within the UK, Europe and outside the European Economic Area in connection with the fulfilment of the applicant's voluntary requests, and the fulfilment of other job opportunities that match the applicant's profile, and confirms that they may be contacted about such job opportunities.