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Assist in coordinating clinical trials from initiation to completion, ensuring adherence to regulations, organizing data, and reporting findings.

The Product Manager defines and improves healthcare technology products, collaborating with stakeholders and ensuring compliance with regulations within an Agile framework.

The Recruitment Specialist II recruits patients for clinical trials through phone screening, schedules appointments, and manages participant relations.

The Regulatory Coordinator I prepares and submits regulatory research documents, maintains credentials, serves as a liaison with IRBs, and supports adherence to regulatory standards.

The Clinical Rater conducts neurocognitive assessments and ratings for study participants, ensuring data integrity and compliance with research protocols.

The Quality Assurance Coordinator ensures data quality and participant safety in clinical trials, supports QA programs, and prepares for audits.

The Pharmacy RN coordinates with pharmacists to support clinical drug trials, dispense medications, maintain records, and ensure compliance with protocols.

Coordinate clinical trial activities from initiation to completion ensuring ICH/GCP compliance; recruit and educate participants; collect and report data, adverse events, and protocol deviations; perform safety assessments (vitals, EKGs, blood draws); assist CTM with vendors, training, and regulatory tasks.

The Laboratory Tech I performs diagnostic testing and laboratory activities, assists in site preparations, monitors inventory, and ensures compliance with regulations.

Ensure adherence to study protocols and quality assurance programs in clinical trials, supporting participant safety and data quality.