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Responsibilities:
- Contribute to one or multiple clinical studies and demonstrate thorough knowledge of clinical operations project management.
- Collaborate with cross-functional clinical study team to support clinical study delivery.
- Evaluates, and ensures appropriate oversight of CROs and other external vendors.
Qualifications:
- At least 5 - 7 years of Clinical Operations experience.
- Bachelor’s degree or higher in a scientific or healthcare discipline preferred and relevant experience within the biotech, pharmaceutical, or CRO industry.
- Extensive knowledge of current ICH-GCP guidelines.
Competencies Include:
- Detail and process orientated, with excellent project management skills, including risk assessment and contingency planning.
- Excellent problem solving, communication and organization skills.
- Ability to work in a collaborative environment and build effective working relationships across the organization.
Nuvalent
Nuvalent is working to create selective medicines designed to address the needs of patients with cancer. They are an exciting early-stage company with experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building.