HCA, Hospital Corporation of America Clinical Project Manager - Work From Home in Nashville, Tennessee

Apply Now! This amazing opportunity is with Sarah Cannon's contract research organization and is a remote based position.

Sarah Cannon Research Institute (SCRI) is the research arm of HCA's global cancer enterprise, Sarah Cannon. Focused on advancing therapies for patients, it is one of the world's leading clinical research organizations conducting community-based clinical trials in oncology, cardiology and orthopedics through affiliations with a network of more than 1,000 physicians across the United States and United Kingdom.

We believe our success is dependent on a healthy work environment where staff members are the core of advancing therapies for patients and accelerating drug development. We apply the same compassion and commitment we have for our patients to our co-workers and colleagues and promote an entrepreneurial culture.

Summary of Key Responsibilities : Coordinating and supervising overall responsibility for multiple assigned clinical research trial project timelines throughout all lifecycle phases. Provide leadership in the development of trials as well and related documents. Will work closely and effectively with physician principal investigator, research directors, clinical trial sponsor, study team and outside consultants.

Duties and Responsibilities : Duties include but are not limited to: * Planning and tracking of all assigned clinical activity in the lifecycle phases of the start up, interim and close out

  • Define and manage project resource needs and establish contingency plans for key resources

  • Planning of trial budget, communicating deviations from trial budget projections and propose solutions for budget delays and deviations

  • Creates integrated project timelines

  • Tracks performance metrics for trial teams

  • Identifies and presents project related issues and facilitates resolutions both in and across function

  • Provide proactive and creative recommendations on how to meet goals and handle identified deviations

  • Develop project status reports and communicates with all applicable team members in and outside the organization

  • Build and maintain strong pharmaceutical industry sponsor and organizational team relationships for the success of clinical trial management

  • Support clinical operations department head to ensure that clinical trial resources are developed, estimated, and reported accurately and timely

  • Promote effective teamwork among functional teams and provide day to day direction for core team

  • Initiate improvements to enhance the efficiency and the quality of the work performed on assigned projects

  • Communicate and escalate unresolved issues at the appropriate time and to the appropriate level of management

  • Ensure all staff adheres to professional standards and SOPs established for clinical research


  • __Knowledge:/A body of information needed to perform a tasks; May be obtained through education, training or experience/

    o Knowledge of FDA guidelines and GCP is required.

    o Knowledge of budgeting and forecasting.

  • __Skills:/The proficiency to perform a certain task /

    o Professional writing and communication skills.

    o Organizational and prioritizing capabilities.

    o Computer skills with ability using clinical trial databases, electronic data capture, MS Access or Excel.

  • __Abilities:/An underlying, enduring trait useful for performing duties /

    o Resourceful with heightened analytical abilities and problem solving skills in a fast paced environment.

    o Interpersonal skills, detailed-oriented and meticulous.

Education: Bachelor's College Degree (4 yr program) Required

Experience: Minimum Required:

  • 3-5 years experience in healthcare research or other science related field

  • 3-5 years experience in project management

  • 3-5 years experience in a clinical trial environment Preferred:

  • 1-3 years experience writing clinical protocols or other technical documents Certifications/License:

  • LPN or RN

  • Research Professional Certification (CCRP) or exam eligibility

Title: Clinical Project Manager - Work From Home

Location: Tennessee-Nashville-Sarah Cannon Research Institute Clinical Operations

Requisition ID: 25319-CPM-SARA