The Division of Genetics and Genomics is seeking an experience coordinator to assist with cutting edge, small scale trials in personalized medicine. The coordinator would be responsible for assisting with budget and protocol development, schedule and running study visits and overseeing overall organization and team workflow and communication. This is a unique opportunity to work on these cutting edge trials. Experience with human subject clinical trials is required. Minimum of a 2 year commitment.
The Clinical Research Specialist II will also be responsible for:
Leading the clinical research study process. Oversees collection, maintenance and retrieval of study data and implementing systems and procedures to ensure accuracy, consistency and conformance with protocol requirements. Acts as a resource to clinical research staff to ensure standards for data management and quality assurance are adhered to in each study.
Assisting Principal Investigators (PIs) in planning and implementing clinical research studies as assigned. Coordinating preparation of protocol applications for submission to the IRB, sponsor or regulatory authority. Corresponding with the IRB, study sponsors, clinical research organizations, study participants and referring physicians.
Recruiting study participants for enrollment in clinical trials. Following individual study protocols. Completing informed consent procedures as assigned. Organizing strategies for recruiting study participants, screening study participants for eligibility on the telephone, in the clinic and other settings as required.
Organizing study procedures and scheduling study participants for study visits. Assisting the PI during patient visits. Performing study procedures designated for the Study Coordinator.
Completing record abstraction of source documents, conducting required study measurements and completing study Case Report Forms in accordance with best practice methods. Conducting a QC check of completed CRFs prior to submission for data entry; coordinating resolution of all data queries. Completing data entry as warranted.
Complying with all institutional policies and government regulations pertaining to human subjects protections. Maintaining regulatory binders, case report forms, source documents, and other study documents. Monitoring the occurrence of clinical adverse events, reporting any to the (PI), the study sponsor and Committee on Clinical Investigations (IRB). Updating protocol and amendment changes.
Conducting the collection or processing of study specimens, delivery to appropriate labs or packaging and shipping to appropriate facilities.
To qualify, you must have:
Bachelor's degree and 5 years of relevant experience OR MS and 2 year relevant work experience.
The proven ability to work independently.
The analytical skills to collect information from diverse sources, apply professional principles in performing various analyses, and summarize the information and data to solve problems.
Communication skills to effectively deal with conflicting views or issues and mediate fair solutions, and well-developed writing skills. Requires effective communication skills with parents/study participants to explain the research protocol, obtain informed consent, obtain accurate information from them, and provide them with accurate information.
Boston Children's Hospital offers competitive compensation and unmatched benefits,
Boston Children's Hospital is an Equal Opportunity / Affirmative Action Employer. Qualified applicants will receive consideration for employment without regard to their race, color, religion, national origin, sex, sexual orientation, gender identity, protected veteran status or disability.
Internal Number: 3041975
About Boston Children's Hospital
Boston Children's Hospital is a 395-bed comprehensive center for pediatric health care. As one of the largest pediatric medical centers in the United States, Children's offers a complete range of health care services for children from birth through 21 years of age.