Opportunities
Project Coordinator
Department: Clinical Operations
Reports to: Project Manager
Overview:The Project Coordinator is responsible for executing the technical functions required by the study protocol and collaborating with the study team to facilitate study success.
Responsibilities:
- Executes technical and clinical functions as required by the study protocol and according to RadPharm' s Standard Operating Procedures (SOPs).
- Prepares images for QA and reading as directed by study protocol and Project Manager/Leader.
- Assists the radiologist in film QA and reads as required.
- Maintains security of images, data and equipment.
- Enters, maintains and tracks data in the computer database
- Ensures confidentiality of study protocols and subjects is maintained.
- Participates in sponsor visits and audits as requested.
- Interacts with all customers appropriately and professionally.
- Reports study needs and issues to the Manager, Clinical Operations.
- Collaborates with management to resolve technical/radiological/study concerns and problems.
- Responsible for his/her continuing professional education.
- Identifies and participates in the performance improvement process.
- Participates in the development, review and evaluation of SOPs and study specific procedures.
- Maintains a safe work environment. Reports workplace hazards immediately.
Qualifications:
- Bachelor's degree in life sciences or pharmaceutical sciences.
- Good working knowledge of GCP and ICH guidelines.
- Medical terminology and knowledge of anatomy and physiology is preferred.
- Excellent organizational and interpersonal skills.
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