MUSC Health

Trial Program Manager

MUSC Health

Charleston, SC, USA
Full-TimeDepends on ExperienceSenior LevelMasters
Job Description

Are you a highly motivated and organized individual with a passion for improving healthcare? Do you have experience managing complex projects and working with diverse teams? If so, we have an exciting opportunity for you to join our team at MUSC Health as a Trial Program Manager.As a Trial Program Manager, you will play a crucial role in the success of our clinical trials by overseeing all aspects of the program from start to finish. This includes coordinating with various departments and stakeholders, ensuring compliance with regulations, and managing budgets and timelines.To excel in this role, you must have a Bachelor's degree in a related field and at least 5 years of experience in clinical trials management. Strong communication and leadership skills are essential, as well as a detail-oriented and results-driven mindset.If you are ready to take on a challenging and rewarding position in the healthcare industry, we encourage you to apply for the Trial Program Manager role at MUSC Health. Join our team and make a difference in the lives of patients through innovative clinical research.

  1. Oversee all aspects of clinical trial programs, including planning, execution, and monitoring.
  2. Collaborate with various departments and stakeholders to ensure smooth and efficient operation of clinical trials.
  3. Ensure compliance with regulations, protocols, and guidelines for all clinical trials.
  4. Manage budgets and timelines for each trial, ensuring efficient use of resources and timely completion.
  5. Develop and maintain relationships with external partners, such as pharmaceutical companies and research organizations.
  6. Lead and motivate a diverse team of researchers, coordinators, and support staff to achieve successful outcomes.
  7. Conduct regular meetings and provide updates to keep all stakeholders informed of progress and any issues.
  8. Work closely with physicians and healthcare professionals to ensure seamless integration of clinical trials into patient care.
  9. Identify and address any potential risks or obstacles to the success of clinical trials.
  10. Monitor and analyze data to make informed decisions and recommendations for improving trial procedures and outcomes.
  11. Ensure ethical and responsible conduct of clinical trials, including protection of patient rights and safety.
  12. Participate in the development and implementation of new clinical trial protocols and procedures.
  13. Maintain accurate and up-to-date documentation of all trial activities.
  14. Stay current with industry trends and developments related to clinical trials and make recommendations for improvement.
  15. Serve as a liaison between the clinical research team, other departments, and external partners to facilitate effective communication and collaboration.
  16. Train and mentor new team members and provide guidance to junior staff.
  17. Maintain confidentiality of all sensitive information related to clinical trials.
  18. Demonstrate a commitment to the mission and values of MUSC Health and the importance of clinical research in improving healthcare.
  19. Adhere to all ethical and legal standards for conducting clinical trials.
  20. Continuously evaluate and improve processes to optimize efficiency and quality in clinical trial management.
Where is this job?
This job is located at Charleston, SC, USA
Job Qualifications
  • Bachelor's Degree In A Healthcare-Related Field: A Trial Program Manager At Musc Health Should Have A Strong Foundation In Healthcare, Including Knowledge Of Clinical Trials And Research Protocols.

  • Previous Experience In Clinical Trials Management: Candidates Should Have At Least 3-5 Years Of Experience Managing Clinical Trials, Preferably In An Academic Medical Center Or Research Organization.

  • Knowledge Of Fda Regulations And Good Clinical Practice (Gcp) Guidelines: The Ability To Navigate And Adhere To Regulatory Requirements Is Crucial For Ensuring The Safety And Ethical Conduct Of Clinical Trials.

  • Strong Project Management Skills: The Trial Program Manager Will Be Responsible For Overseeing Multiple Trials Simultaneously, Making It Essential To Have Excellent Organization, Time Management, And Communication Skills.

  • Leadership And Teamwork Abilities: This Role Requires Working Closely With A Multidisciplinary Team, Including Researchers, Physicians, Nurses, And Other Healthcare Professionals. The Ideal Candidate Should Have Experience Leading And Collaborating With Others To Achieve Common Goals.

Required Skills
  • Quality Assurance

  • Strategic Planning

  • Project Management

  • Data Analysis

  • Communication

  • Time Management

  • Budget management

  • Conflict Resolution

  • Team Leadership

  • Risk assessment

  • Stakeholder management

  • Resource allocation

Soft Skills
  • Communication

  • Conflict Resolution

  • Customer Service

  • Emotional Intelligence

  • Leadership

  • Time management

  • creativity

  • Teamwork

  • Adaptability

  • Problem-Solving

Compensation

According to JobzMall, the average salary range for a Trial Program Manager in Charleston, SC, USA is between $65,000 and $90,000 per year. This salary range can vary depending on factors such as experience, education, and the specific industry or company the Trial Program Manager is working for. Additionally, bonuses and other benefits may also be included in the overall compensation package for a Trial Program Manager in Charleston.

Additional Information
MUSC Health is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
Required LanguagesEnglish
Job PostedJanuary 23rd, 2024
Apply BeforeSeptember 18th, 2025
This job posting is from a verified source. 
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