Senior Project Manager in Nashville, Tennessee, United States
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Senior Project Manager

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Nashville, TN, United States
Full-time • Work From Home
Job ID: 6501
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Description

Senior Clinical Project Manager
 
Sarah Cannon Development Innovations is a full-service contract research organization (CRO) that is uniquely focused in oncology. Sarah Cannon Innovations offers strong scientific leadership, access to patients through Sarah Cannon Research Institute’s Site Management Organization (SMO) and relationships with other clinical sites, and experience in drug development and delivery of clinical trials from First-In-Man through registration level studies, making us the partner of choice for oncology.

Sarah Cannon, the global cancer enterprise of Hospital Corporation of America (HCA), offers integrated cancer services with convenient access to cutting-edge therapies for those facing cancer in communities across the United States and United Kingdom.

Benefits:

  • Student Loan Repayment
  • Tuition Reimbursement/Assistance Programs
  • Paid Personal Leave
  • 401k (100% annual match – 3%-9% of pay based on years of service)
  • Identity Theft Protection discounts
  • Auto, Home, and Life Insurance options
  • Adoption Assistance
  • Employee Stock Purchase Program (ESPP)

**This is a Work-From-Home position and you can be located anywhere in the United States to be eligible for this role.Job Summary and Qualifications

As the Senior Clinical Project Manager, you are responsible for the management of multiple clinical trial projects (including global projects) throughout all lifecycle phases. You will ensure project work completion to the client expectations, ensuring quality deliverables on time and within budget and in accordance with SOPs, ICH GCP, applicable laws, regulations, policies and practices. You will serve as the principal liaison with clients to ensure effective and timely communication of project progress, issues, and plans for resolution of those issues, providing leadership in the development of clinical trials and related documents. You will work closely and effectively with cross-functional teams to provide strategy and input in business development proposals and attends bid defenses.

Duties and Responsibilities:

  • You will plan, track and run all activity throughout the project lifecycle, including deliverables from all functional areas and vendors to the project scope
  • You will develop project plans, timelines and status reports and communicates with all applicable team members in and outside the organization
  • You will promote effective partnership among cross-functional teams and provide day to day direction for core team
  • You will meet with team members on a regular basis regarding project tasks to ensure project achievements
  • You will serve as primary project contact with clients
  • You will craft project budgets, communicate deviations from budget projections and propose solutions for budget deviations
  • You will lead problem solving and resolution efforts. You will provide dedicated and creative recommendations on how to meet goals and handle identified risks and deviations
  • You will ensure that work is conducted in compliance with professional standards and SOPs, and meet quality and timeline metrics
  • You will build and maintain strong pharmaceutical industry sponsor and organizational team relationships for the success of clinical trial management
  • You will mentor project managers
  • You will participate in proposal development, bid-defense process and presentations

For this position, you must have:

  • Bachelor’s Degree (4 year program)
  • 5 years of clinical trial experience within pharmaceutical, biotechnology or CRO company managing the logistics of clinical trial conduct, budgeting/forecasting, and developing/executing project plans
  • 5 years of previous experience as a Clinical Project Manager for a CRO/pharma/biotech company
  • Experience in oncology clinical research phases I-III

It is preferred that you have:

  • 7 years of clinical trial experience within pharmaceutical, biotechnology or CRO company
  • 7 years of previous experience as a Clinical Project Manager for a CRO/pharma/biotech company
  • Experience writing clinical protocols and other technical documents
  • Prior experience mentoring and/or training less senior team members
  • Experience managing study timelines, deliverables, and/or vendors

Do you find this opportunity compelling, if so we encourage you to apply? We promptly review all applications. If you are highly qualified you will hear from one of our recruiters. We are actively interviewing so apply today.

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

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    Work from Home
    Full-time • Work From Home

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