What are the responsibilities and job description for the Clinical Study Manager position at RI - Non-Therapeutic?
We are seeking a highly skilled Clinical Study Manager to join our research team at RI - Non-Therapeutic. In this role, you will be responsible for coordinating multiple research protocols and serving as a liaison with local investigators, clinical staff, and research personnel.
Your primary responsibilities will include:
Complete study medication order forms accurately and have physician or appropriate designee sign orders prior to medication administration.
Perform routine operational activities for multiple research protocols.
Liaise between site research personnel, industry sponsors, and Supervisor.
This role requires strong leadership and organizational skills, with the ability to work effectively in a fast-paced environment. You will also need to possess excellent communication and interpersonal skills, with the ability to collaborate closely with various site departments/teams.
Key Responsibilities:
Collaborate closely with various site departments/teams, including finance, relevant hospital administrative representatives, and the local IRB, if applicable.
Schedule Information:
This position is a contract-based role with a duration of 6 months. We offer a competitive compensation package and opportunities for professional growth and development.
