The Regulatory Specialist is responsible for coordinating and participating in all regulatory research activities for all sites across ObjectiveHealth. This will include preparing, reviewing, managing and tracking study-specific regulatory documents and training documentation. This role will also require the maintenance of delegation of authority and training logs, as well as CVs, licenses, training certificates, etc., for key personnel. This individual works closely with the clinical study teams and Research Center leadership to ensure GCP compliance while meeting strict deadlines. A successful candidate is a team player, has prior experience in regulatory management, and is a detail-oriented self-starter.
Who We Are
ObjectiveHealth is a clinical research company that uses proprietary technology to:
All with the goal of Improving Patient Outcomes at the Point of Care. We want you to join us in doing just that.
Key Responsibilities
Qualifications
What We Offer
Competitive compensation, 401(k) with Company match, a clear career pathway for advancement within the Company, Short- and Long-Term Disability, Health Savings and Flexible Spending Accounts, Health, Dental and Vision insurance Plans, Generous PTO, Adoption Assistance, Paid Holidays, and a wide selection of other voluntary benefits.
This job requires legal authorization to work in the US. We are not currently accepting work visas. ObjectiveHealth is an EEO Employer and an E-Verify participant.
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