About the Company
Labcorp Drug Development, formerly Covance, is a leading global contract research organization (CRO) providing comprehensive drug development services. We partner with pharmaceutical and biotechnology companies to bring innovative medicines to patients worldwide. Our commitment to scientific excellence, patient safety, and ethical conduct is at the core of everything we do. Join a team dedicated to making a significant impact on global health.
Job Description
We are seeking an experienced and highly motivated Clinical Trial Manager to join our dynamic team in Scottsdale, AZ. This critical role involves overseeing the operational aspects of clinical trials, ensuring their successful execution from initiation through close-out. The ideal candidate will manage cross-functional teams, maintain adherence to study protocols, and ensure compliance with regulatory guidelines (GCP, ICH). This position is pivotal in delivering high-quality clinical trial data and accelerating the development of life-changing therapies. A comprehensive relocation package is available for qualified candidates.
Key Responsibilities
- Manage and oversee the operational aspects of assigned clinical trials, ensuring timely and within-budget execution.
- Develop, implement, and maintain project plans, timelines, and budgets.
- Lead and motivate cross-functional study teams, including CRAs, CTAs, and other functional leads.
- Ensure trial activities are conducted in accordance with the protocol, standard operating procedures (SOPs), GCP, and ICH guidelines.
- Oversee vendor selection and management, ensuring quality deliverables.
- Identify, assess, and mitigate study-related risks.
- Facilitate communication and collaboration between internal teams, sites, and clients.
- Prepare and present regular trial updates to internal and external stakeholders.
- Review and approve study-related documents, including protocols, informed consent forms, and monitoring plans.
- Participate in the selection, training, and evaluation of clinical research staff.
Required Skills
- Minimum of 4 years of experience in clinical trial management or a similar role within a CRO, pharmaceutical, or biotech company.
- Demonstrated knowledge of Good Clinical Practice (GCP) and ICH guidelines.
- Strong project management skills with the ability to manage multiple priorities.
- Excellent leadership, communication, and interpersonal skills.
- Proficiency in clinical trial management systems and Microsoft Office Suite.
- Bachelor's degree in a life science, healthcare, or related field.
- Ability to travel as required (up to 25%).
Preferred Qualifications
- Master's degree in a relevant scientific or health-related discipline.
- Certification in Clinical Research (e.g., CCRP, PMP).
- Experience in specific therapeutic areas such as Oncology, CNS, or Cardiovascular.
- Experience with global clinical trials.
Perks & Benefits
- Comprehensive health, dental, and vision insurance plans.
- Generous paid time off and holidays.
- 401(k) retirement plan with company matching.
- Life and disability insurance.
- Employee assistance programs.
- Professional development and career growth opportunities.
- Tuition reimbursement program.
- Competitive relocation package available.
- Dynamic and collaborative work environment.
How to Apply
If you are interested in this position, please click the "Apply Now" button below. To ensure your application is properly considered, please prepare the following:
- An up-to-date Resume or CV
- A brief cover letter summarizing your experience and motivation
Applications are reviewed on a rolling basis. Only shortlisted candidates will be contacted for an interview.
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