Clinical Research Coordinator

Two Clinical Research Coordinator (CRC) positions are available in the laboratory of Dr. Javad Nazarian (https://childrensnational.org/research/labs/nazarian/about) at Children’s National Research and Innovation Campus, Children’s National Hospital. This position is expected to play a prominent role within the research program of a brand-new, one-of-a-kind research and innovation hub that drives life-saving discoveries. The ideal candidate is seeking a long-term career within a growing lab, is passionate about applying scientific knowledge in pursuit of a pediatric brain cancer cure, eagerly learns new skills, welcomes new responsibilities, and has excellent time management and project management skills. The CRC will independently lead day-to-day operations of Clinical Research studies, which are conducted by a principal investigator, with limited supervision. In addition, the individual performs a variety of complex duties involved in the collection, compilation, documentation and analysis of Clinical Research data. The CRC will develop progressive functional knowledge of Good Clinical Practices (GCP), Office of Human Research Protections (OHRP) regulations and Food and Drug Administration (FDA) regulations. Basic knowledge of molecular biology is required as The CRC might conduct some bench research as well. The CRC will have the opportunity to work closely with post-doctoral fellows and other research staff, including principal investigators. The CRC may have the opportunity be co-authors on papers commensurate with their contribution.

Required Skills

· Previous experience and knowledge of depositing/accessioning samples into a biorepository

· Experience with collecting and processing a variety of patient biospecimens including (but not limited to) surgical tissue, blood, urine, cerebrospinal fluid

· Extensive familiarity with Clinical Research databases, data collection tools, and clinical data analysis methods

· Ability to manage multiple complex activities while maintaining close attention to details and not losing sight of the organization mission

· Interpersonal skills that demonstrate formal and informal leadership in a diverse professional environment

· Working knowledge of Microsoft Word, PowerPoint, Excel, Outlook, TEAMS

· Basic knowledge of lab safety and use of basic lab equipment required

Record Keeping

· Maintain a log of work performed

· Prepare charts, graphs, and results of studies; compile and help analyze data.

· Maintain all required records, reports, statistics, etc.; prepare summary reports as requested.

Research Administration

· Maintains knowledge and comprehension of assigned research protocols, including study procedures, timelines and eligibility.

· Accurately creates, completes, maintains, organizes and accounts for study materials, including participant lists and visit logs, regulatory binders, case report forms, laboratory kits, investigational product(s) and participation incentives.

· Uses and accounts for research funds and resources at performance level, including reconciling research subject billing if assigned.

· Attends study meetings, which could include overnight travel, as requested by principal investigator.

· Works well with other members of the research team, appreciates a diverse workplace and seeks and provides input when appropriate.

· Serves as an effective liaison between the investigators, sponsors, hospital departments involved with research studies and the Clinical Research Center.

· Identifies and resolves issues and challenges with appropriate input and oversight.

· Creates standard operating procedures (SOPs), and implements operational plans.

· Provides oversight and training to study team members for a variety of studies.

· Develops study documents, including consent forms and protocols.

Study Management

· Conducts/participates in feasibility assessments to ensure adequate site resources and infrastructure are available for protocol participation.

· Plans, conducts and manages research activities in accordance with federal regulations and guidance documents and sponsor and institutional policies under the direction of a senior study team member.

· Ensures regulatory integrity of protocols through the accurate and timely preparation and submission of documents and reports to the sponsor, IRB and other oversight bodies in accordance with federal regulations, sponsor SOPs and institutional policies.

· Authors study submissions and related documents based on functional role; this may include IRB contingency responses, ClinicalTrials.gov postings, Certificate of Confidentiality applications and scholarly presentations and publications.

· Registers and records participant visits in the appropriate tracking system.

· Anticipates study needs and subject caseload to meet organizational objectives and deadlines in a timely manner.

· Coordinates, prepares for and responds to routine oversight body visits and audits.

· Independently authors reports to oversight bodies and/or trains and oversees staff performing these tasks.

Education & Experience

· BS/MS degree in biology or life science related field. Candidates with BS in biology will be considered if they have more than 1 year of research experience.

Salary and Benefits

· The salary range indicated in the job posting on Indeed is not final. This range is generated by the Indeed algorithm and is subject to the decision of the HR team and the Principal Investigator.

Job Type: Full-time

Pay: $20.00 - $25.00 per hour

Expected hours: 40 per week

Experience level:

• 1 year
• 2 years

Medical specialties:

• Oncology

Schedule:

• 8 hour shift
• Monday to Friday

Ability to Relocate:

• Washington, DC 20012: Relocate before starting work (Required)

Work Location: In person