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We have an excellent career opportunity for a Study Director I to join our Vivarium Operations team in Denver, PA.
Position Summary
The Study Director is an individual contributor who is responsible for managing the design, conduct and reporting of non-regulated vaccine immunogenicity and efficacy studies to meet scientific and client requirements. They coordinate efforts of the study team, lead the interpretation, analysis, documentation, and reporting of results which includes productive interactions with management, technical staff, global internal and external clients, and study direction staff.
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Candidates given best consideration will have the following qualifications:
- Knowledge of the drug development processes, and the scientific techniques of vaccine studies.
- Previous data interpretation and report writing experience.
- Strong client relationship building and management skills.
- Excellent organizational and time management skills
- Good verbal and written communication skills
- Ability to help foster a high professional standard and encourage positive staff relationships.
Education/Experience
- Bachelor's degree in Life Sciences or equivalent years of experience, Master's preferred.
- 1 to 4 years of relevant scientific or animal study related experience.
Essential Duties:
- Serve as a Study Director on vaccine immunogenicity and efficacy study designs as determined appropriate by management.
- Coordinates efforts of the study team.
- Ensures that selected study plan/protocols, including any changes, are scientifically robust (with management/senior scientist input as needed), approved by the client, and are in compliance with the appropriate SOPs, and animal welfare guidelines.
- Monitors progress and status of assigned studies with direction from mentor/management/senior scientists. Ensures that all experimental data, including observations of unanticipated responses to the test system, are accurately recorded, and verified.
- Provides excellent customer care to both internal and external clients, including timely production of high-quality protocols, compiled study progress updates, reports, and other client deliverables.
- Liaises with sponsors and other customers in a timely and professional manner on study related matters, with some direction from senior scientists.
- Learns to review cost estimates to ensure that all protocol/amendment driven work scope specifications have been included in the price estimation.
- Participates in and may host client visits.
- Evaluate and interpret nonclinical data with minimal support.
Benefits: All job offers will be based on a candidate's skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. Regular, full-time, or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(K), ESPP, Paid time off (PTO) or Flexible time off (FTO), Commissions, and Company bonus where applicable. For more detailed information, please click here.
Why People choose to work at Labcorp:
At Labcorp, it is our people that make us great - it is what our clients, our partners and, most importantly, what our employees say. Here, you will have the opportunity to collaborate with extraordinary people with diverse viewpoints. You will discover your own outstanding potential as we build an even stronger organization with industry leaders from early development to the clinic and beyond. We help our clients develop medicines that improve health and improve lives of their family and friends.
Labcorp is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic.
We encourage all to apply
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