Clinical Research Coordinator Associate
Clinical Research Coordinator Associate
Job Number: 88961
The Department of Orthopaedic Surgery has an immediate opening for a Clinical Research Coordinator Associate (CRCA) to perform duties related to the coordination of clinical studies within the Female Athlete Program. The Female Athlete Programs which is affiliated with the Human Sports Performance Lab brings together a unique team of athletic trainers, physicians, physical therapists and sports scientists to collaboratively provide the best possible medical care for athletic injuries and illnesses. The director of the Female Athlete Program is a leader in the field and the CRCA will have the opportunity to work closely with the director and fellow coordinators, research assistants, physicians, and therapists that are fundamentally changing the world of sports medicine for female athletes of all ages. To learn more about the Department please visit us at: https://ortho.stanford.edu/
The successful candidate will demonstrate:
- Outstanding communication and relationship building skills;
- Strong attention to detail, and competence to manage multiple priorities and respond effectively with limited guidance;
- Commitment to uphold Stanford University's compliance with federal, state, local, and sponsor regulation; and
- Drive to establish themselves as a leading contributor within the Department of Orthopaedic Surgery and Stanford Medicine.
- Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out.
- Determine eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment strategies.
- Coordinate collection of study specimens and processing.
- Collect and manage patient and laboratory data for clinical research projects. Manage research project databases including data entry, develop flow sheets and other study related documents, and complete study documents/case report forms.
- Ensure compliance with research protocols, and review and audit case report forms for completion and accuracy with source documents. Prepare regulatory submissions, and ensure institutional Review Board renewals are completed.
- Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact.
- Monitor expenditures and adherence to study budgets and resolve billing issues in collaboration with finance and/or management staff.
- Interact with the principal investigator regularly, ensuring patient safety and adherence to proper study conduct.
- Ensure essential documentation and recording of patient and research data in appropriate files per institutional and regulatory requirements.
- Participate in monitor visits and regulatory audits.
* - Other duties may also be assigned
EDUCATION & EXPERIENCE (REQUIRED):
Two-year college degree and two years related work experience or a Bachelor's degree in a related field or an equivalent combination of related education and relevant experience. Research experience preferred, and knowledge of statistics a plus.
KNOWLEDGE, SKILLS AND ABILITIES (REQUIRED):
- Strong interpersonal skills.
- Proficiency with Microsoft Office.
- Knowledge of medical terminology.
CERTIFICATIONS & LICENSES:
Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred.
- Frequently stand, walk, twist, bend, stoop, squat and use fine light/fine grasping.
- Occasionally sit, reach above shoulders, perform desk based computer tasks, use a telephone and write by hand, lift, carry, push, and pull objects that weigh up to 40 pounds.
- Rarely kneel, crawl, climb ladders, grasp forcefully, sort and file paperwork or parts, rarely lift, carry, push, and pull objects that weigh 40 pounds or more.
* - Consistent with its obligations under the law, the University will provide reasonable accommodation to any employee with a disability who requires accommodation to perform the essential functions of his or her job.
Occasional evening and weekend hours.
- Interpersonal Skills: Demonstrates the ability to work well with Stanford colleagues and clients and with external organizations.
- Promote Culture of Safety: Demonstrates commitment to personal responsibility and value for safety; communicates safety concerns; uses and promotes safe behaviors based on training and lessons learned.
- Subject to and expected to comply with all applicable University policies and procedures, including but not limited to the personnel policies and other policies found in the University's Administrative Guide, http://adminguide.stanford.edu.
- Schedule: Full-time
- Job Code: 4644
- Employee Status: Regular
- Grade: G
- Department URL: http://cmgm.stanford.edu/micro/
- Requisition ID: 88961
Location: School of Medicine, Stanford, California, United States
To be considered for this position please visit our web site and apply on line at the following link: stanfordcareers.stanford.edu
Stanford is an equal opportunity employer and all qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other characteristic protected by law.
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