Director, Clinical Science

  • location: Waltham, MA
  • type: Temp to Perm
  • salary: $100 - $125 per hour
easy apply

job description

Director, Clinical Science

job summary:
The Director, Clinical Science, designs and implements clinical trials, including writing medical protocols, creatively working to assess appropriate endpoints and interfacing with Clinical Operations to implement trials. The incumbent would work closely with biometrics group and clinical operations to assure accuracy of clinical data and robustness of study outcomes

 
location: Waltham, Massachusetts
job type: Temporary
salary: $100 - 125 per hour
work hours: 9 to 5
education: Bachelors
 
responsibilities:
  • Integrates relevant scientific findings from the project and the literature, to facilitate research and overcome scientific challenges.
  • Designs and implements clinical trials, including writing protocols, creatively working to assess appropriate endpoints and interfacing with Clinical Operations to implement trials.
  • Interprets data, assess integrity of data and provide scientific summaries.
  • Works closely with biometrics group and clinical operations to assure accuracy of clinical data and robustness of study outcomes.
  • Works closely with Project Head, CSO, Research, Clinical and other project team members to achieve the scientific goals.
  • Identifies CROs or other collaborations that further scientific objectives or apply expertise that is not available in-house.
  • Assists Life Cycle Management, regulatory submission activities, and indication development.
  • Collaborates with, monitor and report CRO based study results to the project team.
 
qualifications:
  • PhD or MD with at least 5 years' clinical trial experience preferred; a Bachelors or Masters in a scientific discipline with at least 10 years' directly relevant industry experience is required.
  • Demonstrated expertise in the design, authoring and successful implementation of clinical protocols and clinical study reports.
  • Strong experience reviewing & interpreting study data/reports and presenting findings to project team members.
  • Excellent organizational, written and oral communications skills.
  • Demonstrated experience in scientific writing.
  • A deep understanding of oncology drug development and experience working in cross-functional teams is highly desirable.
  • Experience across the range of early and late stage clinical development is desirable.
 
skills: Clinical Study Design
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

easy apply

get jobs in your inbox.

sign up
{{returnMsg}}

related jobs