Hybrid Dermatology Clinical Research Coordinator

Abundance Network; Redwood City (CA); Hybride; USD 65 000 - 90 000; Plein temps

Résumé du poste

Stanford University Dermatology seeks an experienced Clinical Research Coordinator Associate (CRCA) to coordinate moderately complex aspects of one or more clinical studies under the PI and CR manager. In-person attendance is required between Redwood City and Palo Alto sites.

The role supports federal and non-federal studies, including dermatological and biomedical research focused on bench-to-bedside treatment, with a hybrid work arrangement three to four days per week on the RWC campus.

Qualifications

• Bachelor’s degree in medicine and/or scientific field (biological sciences, social sciences, etc.).
• Three years of clinical research experience preferred.
• Clinical research project management experience.
• Experience with protocols and regulatory bodies (HIPAA, FDA, IRB, GCP).
• Ability to work independently and take ownership of a project.
• Ability to work collaboratively in a team environment.
• Ability to work in a fast-paced environment with multiple projects and timelines.
• Strong oral and written communication skills.
• Detail-oriented with excellent organizational skills.
• Fluency in Spanish is a plus.

Responsabilités

• Serve as primary contact with research participants, sponsors, and regulatory agencies, coordinating studies from start-up through closeout.
• Determine eligibility and gather consent from study participants according to protocol.
• Coordinate collection of study specimens and processing.
• Collect and manage patient and laboratory data for clinical research projects; manage study documents and case report forms.
• Ensure compliance with protocols and regulatory requirements; prepare regulatory submissions and IRB renewals.
• Assemble study kits, monitor scheduling of procedures, and attend monitoring meetings with sponsors.
• Monitor expenditures and adherence to study budgets; resolve billing issues with finance/management staff.
• Interact with the principal investigator to ensure patient safety and proper conduct.
• Ensure proper documentation and recording of data per regulatory requirements.
• Participate in monitor visits and regulatory audits.

Connaissances

Clinical research experience

Project management

Regulatory compliance

Independent work

Team collaboration

Communication skills

Attention to detail

Formation

Bachelor’s degree in biological sciences

Outils

Microsoft Office

Description du poste

Stanford University Dermatology seeks an experienced Clinical Research Coordinator Associate (CRCA) to coordinate moderately complex aspects of one or more clinical studies under the PI and CR manager. In-person attendance is required between Redwood City and Palo Alto sites.

The role supports federal and non-federal studies, including dermatological and biomedical research focused on bench-to-bedside treatment, with a hybrid work arrangement three to four days per week on the RWC campus.