Senior PM - Multi-Center Clinical Trials (Remote)

Hugh Chatham Memorial Hospital; Charlotte (NC); Remote; USD 46,000 - 68,000; Full time

Benefits offered by this job

Paid Time Off

Health and welfare benefits

Educational Assistance Program

Retirement plan with employer match

Job summary

Advocate Health, headquartered in Charlotte, NC, seeks a senior study manager to oversee multi-center trials, coordinate administrative activities, and ensure timely completion of complex research projects. The role emphasizes leadership, budget oversight, and liaison with sponsors and investigators across sites.

Qualifications include a Master's degree in a health-related field and supervisory experience. Remote work is allowed with normal business hours; full-time employment with comprehensive

Qualifications

• Master's degree in Psychology, Nursing, or Basic Science with two years' relevant administrative and medical experience in research projects or other health-related activities; or, an equivalent combination of education and experience.
• One-year experience in a supervisory capacity.

Responsibilities

• Oversees the operational activities at the clinical site(s) and coordinates the activities of a multi-center study or multiple large studies.
• Collaborates with principal investigator(s) in developing plans for research projects and to discuss the interpretation of results. Negotiates protocol changes with funding agency/sponsor.
• Assumes major responsibility for the successful and timely completion of the tasks that comprise the implementation and analysis phases of a multi-center study or multiple studies including planning, development, implementation, and evaluation.
• Coordinates the hiring of and provides direction to support staff. Plans and coordinates training sessions for project personnel located at the different clinical sites. Oversees recruitment, data collection, and follow-up activities.
• Translates planning and design decisions into concrete activities and tasks for project implementation and sets priorities for project implementation.
• Evaluates and interprets collected clinical data. Manages the preparation of progress reports and quality control monitoring; participate in the analysis of study data and the writing of scientific papers for publication.
• Develops data collection forms, procedural manuals, and other documents required for project implementation and evaluation.
• Ensures that all aspects of the following are completed: a. Study is conducted in accordance to the study protocol and contract b. Legal aspects adhere to state and federal regulations and guidelines c. Requirements of the Medical School and the University comply with the conduct of the study d. Technical requirements of the funding agency are met, including auditing requirements
• Conducts site visits to evaluate staff and study activities. Coordinates sponsor audits.
• Represents the project to all related community agencies and organizations, serving as the study's liaison, spokesperson, and representative.
• Conducts meetings and visits with potential study sponsors to promote WFUHS as a study site.
• Attends and participates in national and local meetings related to the planning, operation, and evaluation of the study.
• Assists industry representatives (pharmaceutical, device, etc.) in planning and implementing future studies due to extensive knowledge in the specific field of research.
• Responsible for developing and monitoring the study budget(s). Compiles and prepares financial progress reports. Tracks payments by sponsors, assuring correct amount received for each participant and testing.
• Performs other related duties incidental to the work described herein.

Skills

Communication skills

Scientific principles

Multi-center studies

Education

Master's degree in Psychology, Nursing, or Basic Science

Job description

Advocate Health, headquartered in Charlotte, NC, seeks a senior study manager to oversee multi-center trials, coordinate administrative activities, and ensure timely completion of complex research projects. The role emphasizes leadership, budget oversight, and liaison with sponsors and investigators across sites.

Qualifications include a Master's degree in a health-related field and supervisory experience. Remote work is allowed with normal business hours; full-time employment with comprehensive