Shriners Children’s is an organization that respects, supports, and values each other. We are engaged in providing excellence in patient care, embracing multi-disciplinary education, and research with global impact. We foster a learning environment that values evidenced based practice, experience, innovation, and critical thinking. Our compassion, integrity, accountability, and resilience define us as leaders in pediatric specialty care for our children and their families.

All employees are eligible for medical, dental and vision coverage on their first day! In addition, upon hire all employees are eligible for a 403(b) and Roth 403 (b) Retirement Saving Plan with matching contributions of up to 6% after one year of service. Employees in a full-time or part-time status (40+ hours per pay period) will also be eligible for paid time off, life insurance, short term and long-term disability and the Flexible Spending Account (FSA) plans. Additional benefits available to full-time and part-time employees include tuition reimbursement, home & auto, hospitalization, critical illness, pet insurance and much more! Coverage is available to employees and their qualified dependents in accordance with the plans. Benefits may vary based on state law.

We are a premier pediatric specialty, research, and academic teaching hospital with a medical and research partnership with Massachusetts General Brigham. It is the world’s leading center for pediatric burn care and is the only American Burn Association (ABA) exclusively pediatric verified burn center in New England and New York.

The Boston Shriners Hospital is one of four pediatric burn specialty hospitals in Shriners Children’s health system and provide comprehensive care for cleft lip and palate, as well as other craniofacial anomalies, with a multidisciplinary care team.

• Develops a contemporary knowledge of clinical research regulatory requirements. Has a working knowledge of clinical research process, from protocol development to implementation.
• Supports the investigators’ development of SHC investigator-initiated research protocols. Assists with the analysis of proposed research projects in order to determine appropriateness and feasibility at the local site, including the evaluation of resources required and regulatory requirements.
• Supports the implementation of approved research protocols. Ensures studies are conducted in compliance with the approved protocol, Good Clinical Practice (GCP) guidelines, applicable regulatory requirements, SHC policies and standards. Performs study-specific research activities and/or interventions, within the bounds of professional licensure.
• Responsible for oversight and documentation of the delivery, storage, and disposition of investigational products at the site, in accordance with federal and state regulations and sponsor requirements. Effectively provides information about the use of investigational products to patients. Understands and adheres to safety monitoring and reporting requirements of regulatory agencies that oversee use of an investigational product in research.
• Responsible for tracking all aspects of projects including all study, investigator and Institutional Review Board (IRB) information and 30 % patient recruitment activity.
• Actively collaborates with applicable headquarters departments, including Research Programs, Legal, and Compliance related to protocol reviews, IRB submissions, sponsored contracts, material transfers, data use agreements, and HIPAA compliance for projects conducted within SHC. Works closely with investigators, research leadership, study sponsor and regulatory agencies to conduct, and report the results of clinical research.
• Coordinates the collection of data throughout a clinical study including (1) timely data collection, (2) ensuring accurate data entry into secure research databases. (3) verifying data accuracy through internal quality control measures to confirm reported study data is accurate, complete, and verifiable from source documents.
• Participates data cleaning & database lock procedures in preparation for data analysis; provides timely responses to data queries, addresses data discrepancies, and reviews source documents.

Bachelors Clinical Research, science or other healthcare related field Preferred.

One (1) year plus of relevant research experience, e.g. site management, study management, research regulatory experience, data collection, compliance or other applicable experience

CCRP or CCRC certification strongly preferred, not required