Worldwide Clinical Trials

Clinical Study Manager (San Antonio, Tx)

Worldwide Clinical Trials • $60K — $119K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • University/college degree in life sciences or equivalent certification/experience
  • Minimum of five years in clinical pharmaceutical industry
  • Proven expertise in clinical project management
  • Ability to manage multiple priorities effectively
  • Strong leadership and teamwork skills
  • Excellent communication and organizational abilities

Responsibilities

  • Lead project team members and facilitate their success
  • Coordinate cross-unit activities with stakeholders and subcontractors
  • Manage project resource needs and develop contingency plans
  • Ensure projects are designed, implemented, and tracked effectively
  • Foster teamwork and resolve conflicts among team members
  • Communicate effectively with CSM Management regarding project matters

Benefits

  • Inclusive and equitable workplace culture
  • Commitment to pay equity and transparency
  • Competitive benefits package based on location
  • Support for career development and growth opportunities
  • Opportunity to make a meaningful impact on patients' lives
Full Job Description
What the Clinical Study Manager does at Worldwide

The Clinical Study Manager (CSM) will manage one or more allocated Phase I through IV Clinical Trials that may be local, regional or global in scope. Worldwide Clinical Trials (WCT) Clinical Study Managers are 100% accountable for the success of their projects: Clinical Study Manager (CSM) is responsible for the overall coordination and management of clinical trials from start up through close out activities. Directs the technical, financial and operational aspects of the projects to secure the successful completion of clinical trials. Works with functional area leads to identify and evaluate fundamental project requirements, interpret data on complex issues, is responsible for contingency planning and implementation of rescue strategy where needed and ensure solutions are implemented.

The CSM works to ensure that all project deliverables meet the customer's time/quality/cost expectations. The CSM, with support from the Project Management Directors, working in collaboration with other functional area leads, is accountable for ensuring that all project deliverables meet the customer/contract expectations. The Clinical Study Manager works under the direct supervision and guidance of the Site Director. He/she is not responsible for supervising other staff.

What you will do

  • Lead core project team members and facilitate their ability to lead extended/complete project team
  • Lead cross unit coordination both internal and external, inclusive of sub-contractors
  • Define and manage project resource needs in conjunction with functional heads and establish contingency plans for key resources
  • Ensure successful design, implementation, tracking and revision of project plans for assigned projects
  • Promote effective teamwork among project team members; resolve conflicts as needed
  • Ensure appropriate communication on project-related matters with the CSM Management


What you will bring to the role

  • Experience in managing projects in a multi-office environment
  • Demonstrated ability to handle multiple competing priorities; utilize resources effectively
  • Demonstrated ability to inspire effective teamwork and motivate staff within a matrix system
  • Demonstrated ability to lead by example and to encourage team members to seek solutions
  • Excellent communication, planning and organizational skills
  • Self-motivated and excellent problem solving skills


Your experience

  • Required: University/college degree (life science preferred) or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology) or equivalent combination of education and experience that provides the individual with the required knowledge, skills and abilities


  • Preferred: Minimum of five (5) years of clinical pharmaceutical industry experience including demonstrated skills and competency in clinical project management tasks


At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation.

The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):

United States of America - $60,000.00 - $119,000.00

The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.

We love knowing that someone is going to have a better life because of the work we do.

To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.

About Worldwide Clinical Trials

Worldwide Clinical Trials is a global contract research organization (CRO) that provides clinical research services to pharmaceutical and biotechnology companies. They specialize in early phase development, late phase development, and full-service clinical research. Worldwide Clinical Trials has experience in a wide range of therapeutic areas, including oncology, neuroscience, and infectious diseases. They are committed to providing high-quality, efficient, and cost-effective services to their clients.
Learn more about Worldwide Clinical Trials
Size
1,500 employees
Industry
Founded
1986

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