Teams at Science 37

Coordinates pharmaceutical-sponsored clinical trials from startup through closeout, including participant recruitment, screening, informed consent, enrollment, follow-up, protocol compliance, data collection, adverse-event documentation, regulatory record maintenance, monitoring, and auditing. Collaborates with investigators, project managers, sponsors, vendors, and multidisciplinary teams to meet enrollment and retention goals. May support hybrid trial planning, temporary project management, process improvement, CRC mentorship, and participant education while ensuring GCP, FDA, HIPAA, and SOP compliance.

Lead B2B sales for eClinical solutions by identifying and securing new business, managing pipeline, developing strategic plans and presentations, collaborating cross-functionally, supporting marketing and CRM activities, and traveling up to 50%.