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Job summary
A leading clinical research organization in the United States is seeking an experienced professional to assist in the operational conduct of clinical studies. The ideal candidate will have over 7 years of pharmaceutical or clinical drug development experience and at least 2 years of experience leading global studies. Strong project management skills and proficiency in Microsoft Office are essential, with an emphasis on communication. Oncology experience will be beneficial for success in this role.
Qualifications
At least 7 years of experience in pharmaceutical or clinical drug development.
2 years experience leading global studies.
Demonstrated oral and written communication skills.
Proficiency in Microsoft Office (Outlook, Word, Excel, and PowerPoint).
Responsibilities
Assist the SM Study Lead and study team with operational conduct of clinical studies.
Support a single study or multiple studies.
Lead a study with limited scope.
Track study timelines and proficiently use project management tools.
Interact with internal and external stakeholders.
Skills
Project management
Communication skills
Proficiency in Microsoft Office
Tools
Microsoft Office
Job description
A leading clinical research organization in the United States is seeking an experienced professional to assist in the operational conduct of clinical studies. The ideal candidate will have over 7 years of pharmaceutical or clinical drug development experience and at least 2 years of experience leading global studies. Strong project management skills and proficiency in Microsoft Office are essential, with an emphasis on communication. Oncology experience will be beneficial for success in this role.