Clinical Trial Specialist

*Perform internal and external feasibilities, qualify potential sites and investigators
*Check study specific site identification lists against internal DB and perform internet investigation to assure highest quality of selected sites.
*Support and/or perform submissions to Ethics Committees and/or Regulatory Authorities; ensure tracking of process and follow up of applications.
*Review and approve country/site specific ICF.
*Negotiate Clinical Site Agreements and the payments related to them. Communicate actions between Investigational sites, investigators, CSA Lead and the Clinical Research Associates (CRAs)
*Arrange and track payments related to Clinical Site Agreements.
*Organize process for obtaining translations as required.
*Support other clinical study start-up activities as required to ensure that the clinical deliverables are met.
*Maintain a working knowledge of, and ensure compliance with applicable ICH-GCP Guidelines
*Attend staff meetings and clinical training sessions as required by the worldwide curriculum.
*Participate in project team meetings/trainings (as appropriate), and maintain relationships with other departments/clients as necessary to achieve start-up deliverables.

Experience/Skills:

*Life science degree
*Excellent interpersonal, verbal and written communication skills.
*Good IT skills
*Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail.
*Willingness to work with multiple supervisors in a matrix environment, and to value the importance of teamwork.

Please send your CV to [Email hidden] to apply
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