Join Our Team at Clinitiative Health Research

Clinitiative Health Research, a trailblazer in the clinical trial sector, is currently searching for a dynamic Clinical Data Integration, Coordinator to enhance our operations. Situated in the United States with a broad international presence, we link leading pharmaceutical firms and Clinical Research Organizations (CROs) with premier investigators and clinical research sites worldwide. Our mission is to boost the success rates of clinical studies by crafting strategic partnerships. This role offers the unique opportunity to work alongside top industry professionals in a vibrant, innovative environment.

Job Overview

The Clinical Data Integration, Coordinator plays a critical role in managing the flow of information across our Clinical Feasibility Engagement and Client Success Teams. This position focuses on the efficient handling, review, and processing of study details to ensure optimal matching of clinical research sites for upcoming trials. The ideal candidate will possess a strong background in clinical trials along with excellent organizational and communication skills.

Key Responsibilities

• Information Provision: Act as a key communication point, ensuring smooth information transfer between internal teams.
• Information Reception and Review: Methodically receive, assess, and record study summaries using our advanced CRM systems.
• Detailed Assessment: Match clinical trials with suitable research sites based on specific study requirements.
• Protocol Preparation: Prepare and maintain confidential protocols and study details for site evaluation.
• Database Management: Keep detailed records in our databases to facilitate client interactions and triage.
• Presentation Planning: Develop presentations that clearly depict potential research sites for clinical studies.
• Briefing Preparation: Create detailed briefings for client discussions, enhancing decision-making processes.
• Feasibility Management: Handle the distribution and follow-up of study-related questionnaires and surveys.
• Feasibility Submission: Timely submission of feasibility data during the site selection phase.
• Information Upkeep: Maintain up-to-date, accurate records and ensure efficient data exchange within deadlines.

Qualifications

Applicants should have a solid understanding of the clinical research and trial process, preferably with direct site experience. You should possess:

• A Bachelor’s degree in Life Sciences, Healthcare Administration, or a closely related field.
• At least 2-3 years of experience in clinical research, with a focus on coordination and information management.
• Strong database management skills and a commitment to maintaining data security.
• Exceptional organizational abilities and adeptness in managing multiple tasks simultaneously.

What We Offer

Clinitiative offers a vibrant role at the core of our operations, prominently positioned to significantly impact the success and efficiency of our clinical trials. We provide ample opportunities for career growth and professional development within a supportive setting. Our competitive compensation package includes a comprehensive benefits scheme, designed to support and reward our team members.

If you’re ready to make a substantial impact in a cutting-edge company, apply to Clinitiative Health Research today and help shape the future of clinical trials globally!