Precision is seeking Clinical Project Managers to join a variety of our client's clinical teams. This is an excellent opportunity for someone with strong organizational skills and the ability to work on a variety of tasks and projects simultaneously with minimal supervision. In addition, the successful candidate must have good judgment, be flexible when different tasks arise and be detailed oriented.
Responsibilities
Responsibilities
- Work with the clinical team to support design, development, execution, and delivery of the clinical study in accordance with the clinical development plan/strategy and timelines.
- Collaborate closely with the Sr. Director of Clinical Operations, working on execution and oversight of clinical trials.
- Lead in the oversight of CRO activities and other clinical vendors to ensure study quality meets regulatory requirements.
- Manage multiple vendors to ensure quality operations.
- Support the Sr. Director of Clinical Operations in reviewing and approving regulatory documents and activating clinical sites.
- Manage escalation of study-related issues and communicate as appropriate, with leadership and other functions.
- Anticipate potential study issues and prepare contingency plans with minimal oversight.
- Collaborate with the cross-functional teams on clinical activities (drug supply, resolution of data queries, etc.) and on selection and management of clinical vendors.
- Maintain knowledge of the therapeutic area, current medical practice, and pharmaceutical regulations in order to ensure best practice across all activities.
- Work with the clinical team to support design, development, execution, and delivery of the clinical study in accordance with the clinical development plan/strategy and timelines.
- Collaborate closely with the Sr. Director of Clinical Operations, working on execution and oversight of clinical trials.
- Lead in the oversight of CRO activities and other clinical vendors to ensure study quality meets regulatory requirements.
- Manage multiple vendors to ensure quality operations.
- Support the Sr. Director of Clinical Operations in reviewing and approving regulatory documents and activating clinical sites.
- Manage escalation of study-related issues and communicate as appropriate, with leadership and other functions.
- Anticipate potential study issues and prepare contingency plans with minimal oversight.
- Collaborate with the cross-functional teams on clinical activities (drug supply, resolution of data queries, etc.) and on selection and management of clinical vendors.
- Maintain knowledge of the therapeutic area, current medical practice, and pharmaceutical regulations in order to ensure best practice across all activities.
- ASAP Start
Company:Precision Life SciencesLocation:- - USJob Types:OtherPost Date:January 17, 2022Valid Through:February 17, 2022