Site Identification Project Manager (Clinical Trial Research)
Opportunity Type: Job Opportunities, Public Health OpportunitiesLocation: Remote, US and UK
Salary: Not provided
Opening Date: March 02, 2017
Closing Date: October 01, 2019
Website: https://www.indeed.com/viewjob?jk=91b0a3a6744e733b&q=Public+Health&l=Home+Based&tk=1ba9njo191d91d6h&from=ja&alid=57d83c810cf2df9f36cffbf6&utm_source=jobseeker_emails&utm_medium=email&utm_campaign=job_alerts
The Site Identification Project Manager (SIPM) has the primary responsibility of developing clinical trial site lists for new and existing projects. The SIPM develops appropriate strategies for site selection and manages the site identification process. Utilizing trial proposals and protocols, the SIPM analyzes the study requirements and uses data management skills to determine which sites and investigators are best suited for the trial.
Responsibilities
The Site Identification Project Manager (SIPM) is responsible for owning and achieving interim and final contractual deliverable target site list for awarded programs. The SIPM leads and directs cross-functional teams, understands and manages internal and external client expectations/needs to achieve client satisfaction. The SIPM proactively identifies, resolves/mitigates and escalates risks with site identification and/or issues. The SIPM adheres to PRA standard procedures and processes. The senior SIPM may act as supervisor of the Site Identification Project Analysts. The SIPM may provide oversight to other members of the project management group.
Acts as primary liaison with the TE team and client:
- Oversees site list development
- Provides rational for recommended sites
- Provides metrics for SRQ responses to identify potential accrual risks for the protocol
Ensures adherence to company SOP, policies and guidelines at the project level. Develops the Site Recruitment Questionnaire (SRQ) with support from the assigned TE Develops scoring methodology to assist in site selection based on responses to the SRQ.
In addition to the above:
- Mentoring of other members of the project management team or functional leads, as required
- Proactively identify, recommend and implement processes and systems that add efficiency and accuracy to current methods
- Manage Site Identification Project Analyst
- Serves as primary contact to key Networks and SMOs
Qualifications
- Bachelor’s degree – Undergraduate degree in allied health, science, information systems, or related field/or equivalent experience
- Minimum 3 years of experience in clinical research, including a management role as a team lead or project manager experience
- MS office suite; proficiency with Excel and Power Point is required experience in analytic methods and/or data mining and processing
- Experience working in a Clinical Research Organizations (CRO), clinical trial site or pharmaceutical company
- Experience in roles such as Clinical Research Coordinator/Study Coordinator, Study Start-up, Proposals, Feasibility
- Read, write and speak English; fluency in host country language required
Location
This is a home-based role and can be located in multiple locations throughout the US and UK.
PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.