Responsible for the effective management of all aspects of Investigator-initiated Trials (IITs) including implementation in multi-institutions and research settings in accordance with FDA regulations and Good Clinical Practice guidelines
Job Summary
Responsible for the effective management of all aspects of Investigator-initiated Trials (IITs) including implementation in multi-institutions and research settings in accordance with FDA regulations and Good Clinical Practice guidelines.
Act as the Medical Internal Review Committee (MIRC) lead, reviewing submitted proposals and protocols, adjudicating revisions, setting agendas, developing content, and creating meeting minutes.
The company offers a comprehensive benefits package including Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness, with opportunities for bonus, equity, and stock purchase.
Matching Summary
Responsible for the effective management of all aspects of Investigator-initiated Trials (IITs) including implementation in multi-institutions and research settings in accordance with FDA regulations and Good Clinical Practice guidelines.
Salary
$160,100.00 - $210,100.00 annually; Bonus/Equity: Eligible for annual bonus plan and discretionary equity awards; Benefits: Comprehensive benefits package
Skills & Requirements
Must-have
Investigator-Initiated Trials management
FDA regulations and GCP
multi-institution implementation
cross-functional collaboration
vendor management
protocol review and adjudication
Nice-to-have
highly motivated
collaborative
passionate interest in fighting cancer
strong interpersonal skills
effective professional communications
Key Requirements
MD/PharmD with 4+ years experience
Masters Degree with 6+ years experience
Bachelors Degree with 8+ years experience
Strong project management skills
Ability to plan, prioritize, and execute multiple projects