IQVIA

Serve as a Data Operations Coordinator for one protocol with less then 5 operations staff or 15+ easy to moderately complex central laboratory studies.

Bachelors Degree in life sciences or other related field required. Prepare and distribute status, tracking and project finance reports, and assist the project manager with budget allocation and approval of invoices.

Coordinate for lab samples collection and logistics; review of lab reports and update PI. Review & implement appropriate recruitment/referral activities for active enrollment at sites.

Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.

Provide comprehensive data management expertise to Data Management team to provide high quality data management products that meet customer needs.

Consult with clients, external IQVIA divisions, and Clinical Pharmacology staff on study design, or other aspects of Clinical Pharmacology projects, and clinical development plans.

To Prioritize and complete the assigned trainings on time. Process Safety data according to applicable regulations, guidelines, Standard Operating procedures and project requirements.

Perform monitoring and site management work to ensure that sites are conducting the studyies and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Sales ability, persuasiveness, use of appropriate interpersonal style and communication methods to facilitate an acceptance of an idea, plan, activity or product from targeted customers. Establishes account plans based on customer needs and business priorities.