Clinical Program Leader in Cambridge, MA at DISYS

Date Posted: 10/12/2018

Job Snapshot

Job Description

o Provides subject matter expertise and operational input into protocol synopsis and final protocol document

o Challenges study team to ensure operational feasibility, inclusive of patient and site burden

o Validates budget and ensures impacts are adequately addressed

o Participates in country and site selection process, with a focus on providing country insights, corporate alignment and therapeutic expertise to ensure alignment between study execution plan and program strategy

o Challenges study team to ensure timelines meet the needs of the clinical development plan  This position offers a strong benefits package including health and life insurance.  There is also a generous PTO package.  Work life Balance is appreciated and respected!

Job Requirements

5+ years’ experience in pharmaceutical industry and/or clinical research organization, including 3+ years clinical study management strongly preferred.

Experience must include early phase clinical studies or Phase 2 and 3 studies and global/international studies or programs.

Experience in more than one therapeutic area is advantageous. 



Digital Intelligence Systems, LLC. is an Equal Opportunity Employer, M/F/D/V. We do not discriminate against any employee or applicant because they inquired about, discussed, or disclosed compensation. Email recruitinghelp @ disys.com to contact us if you are an individual with a disability and require accommodation in the application process.
Digital Intelligence Systems, LLC. is an Equal Opportunity Employer, M/F/D/V. We do not discriminate against any employee or applicant because they inquired about, discussed, or disclosed compensation. Email recruitinghelp @ disys.com to contact us if you are an individual with a disability and require accommodation in the application process.