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Atrium Health Wake Forest BaptistPosted 30+ days ago

Project Manager II - NCCT Study Start-up Navigator

Full-time
Remote
2+ years
Competitive
Posted 30+ days ago

Atrium Health Wake Forest Baptist seeks a Project Manager II to plan, develop, implement, and evaluate multi-center clinical studies or multiple large studies. The role coordinates clinical-site operations, study personnel, data collection and analysis, regulatory compliance, sponsor relationships, and study budgets.

Posted
30+ Days Ago
Source
jobs.talemetry.com
Sector
Healthcare

Opens the employer's application page in a new tab

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

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
  • Excellent oral and written communication skills
  • Demonstrates knowledge of scientific principles
  • Experience in both single- and multi-center studies

Required skills

Scientific PrinciplesStaff Supervision

Nice to have

Oral and Written Communication

Full job description

Atrium Health Wake Forest Baptist seeks a Project Manager II to plan, develop, implement, and evaluate multi-center clinical studies or multiple large studies. The role coordinates clinical-site operations, study personnel, data collection and analysis, regulatory compliance, sponsor relationships, and study budgets.

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

Benefits

  • Remote
  • Premium pay such as shift, on call, and more based on a teammate's job
  • Incentive pay for select positions
  • Opportunity for annual increases based on performance
  • Paid Time Off programs
  • Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability
  • Flexible Spending Accounts for eligible health care and dependent care expenses
  • Family benefits such as adoption assistance and paid parental leave
  • Defined contribution retirement plans with employer match and other financial wellness programs
  • Educational Assistance Program

Company

  • Academic medical center and health system
  • Winston Salem, North Carolina, USA
  • https://www.wakehealth.edu/
  • Founded in 1902
  • 10001+ employees

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
  • Excellent oral and written communication skills
  • Demonstrates knowledge of scientific principles
  • Experience in both single- and multi-center studies
  • 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.

Required skills

  • , Scientific Principles, Staff Supervision

Preferred skills

  • Oral and Written Communication

Experience

  • 2+ years

Job details

Employment type

Full-time

Seniority level

2+ years

Date posted

Oct 13, 2026

Work mode

Remote

Job source

jobs.talemetry.com

Company

Atrium Health Wake Forest Baptist

Healthcare

Academic medical center and health system

See all 2 jobs from Atrium Health Wake Forest Baptist →
  • Winston Salem, North Carolina, USA
  • Healthcare
  • 10001+ employees
  • Founded 1902
  • wakehealth.edu

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