Clinical Data Integration Specialist

2 weeks ago


New York, New York, United States Clinitiative Health Research Full time
Job Title: Clinical Data Integration, Coordinator

Clinitiative Health Research is a pioneering force in the clinical trial industry, connecting top-tier pharmaceutical companies and Clinical Research Organizations (CROs) with distinguished principal investigators and clinical research sites.

We are committed to enhancing the success rates of clinical studies through strategic partnerships and bespoke business development solutions tailored to the intricate needs of our clinical research site clients.

As a Clinical Data Integration, Coordinator, you will collaborate closely with industry-leading pharmaceutical firms and CROs, driving innovation and excellence in clinical research.

Key Responsibilities:
  • Facilitate the flow of information between the Clinical Feasibility Engagement and Client Success Teams.
  • Receive, review, and process study summaries and details to ensure our clinical research sites are well-matched to the requirements of upcoming trials.
  • Ensure efficient and accurate transfer of information within the organization and maintain strict timelines for all processes.
  • Create blinded protocols and study details for site review to maintain confidentiality during the site selection process.
  • Develop a blinded or unblinded site list that clearly outlines potential sites for studies based on detailed assessments.
  • Prepare comprehensive briefings for the Client Success team Liaison, including the study plan and selected client clinical research sites.
  • Enter all client-received feasibility information into designated sponsor/CRO platforms during site selection within pre-determined timelines.
Requirements:
  • Familiarity with clinical research and the clinical trial process.
  • Site experience is preferred.
  • Excellent communication skills and the ability to manage complex information flows within an organization.
  • Proficiency in database management and information security practices.
  • Ability to create detailed reports and presentations.
  • Highly organized with a keen attention to detail and the ability to manage multiple competing tasks simultaneously.
  • Proactive in ensuring timely completion of tasks and adherence to deadlines.
What We Offer:

A role at the heart of our operations, with a significant impact on the success and efficiency of our clinical trials.

Opportunities for career advancement and professional growth in a supportive environment.

Competitive salary and comprehensive benefits package.



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