Staff Research Associate I

Ncire•San Francisco, CA

4d•Onsite

About The Position

The Staff Research Associate I is responsible for participating in the day-to-day operations of routine, minimally complex clinical research programs and/or studies conducted by Principal Investigators (PIs) at the San Francisco VA. Performs a variety of administrative and operational duties involved in the collection, compilation, documentation, and review of clinical data. Supports the achievement of research program and/or study objectives. Works under close supervision, receiving instruction, guidance and direction from Senior staff research associates, Clinical Research Supervisor and/or leadership team. We are looking for a professional, team-motivated, detail-oriented individual to provide support for both new and ongoing research projects on the Hematology Oncology Research Team here at the SFVA! These projects encompass industry and/or PI-initiated studies focusing on precision oncology.

Requirements

B.A. / B.S.
Prior experience with research in the hard sciences, clinical sciences, or social sciences, including prior academic research experience, e.g. college-level research
Strong oral/written communication, interpersonal and organizational skills
Experience with word processing and database software, such as Microsoft Access and Excel
Proficiency in conducting literature searches
Ability to work independently as well as part of a team
Ability to manage multiple tasks and priorities to achieve desired goals
Excellent organizational skills
Strong attention to detail

Responsibilities

Prepares and takes part in site initiation, monitoring, closeout visits, document storage activities, and related training. May assemble the necessary parties to ensure that all required agreements are in place.
Utilizes and assists senior team members on electronic data capture systems, technologies, and software necessary for clinical research program and/or study operations.
Scores tests, enters data, and completes required forms accurately and according to protocol.
Assists with the development of data collection documents and instruments, maintains subject level documentation, and prepares documents, equipment and/or supplies identifies issues recommends solutions.
Conducts study specific procedures including but not limited to: Consenting patients for non-interventional research studies, Interviewing patients, Generating patient correspondence.
Submits assigned studies for review and approval and provides status updates throughout the startup process.
Assists regulatory team with Institutional Review Board (IRB) preparation and submission.
Screens, schedules, consents participants in assigned clinical research programs and/or studies.
With guidance, explains the difference between clinical activities and research activities, risk and benefits of study participation to participants.
Engages with senior study team to maintain participant recruitment and retention rates and assists with participants with individual needs, collects information to determine feasibility.
Collects information to determine feasibility, recruitment, and retention strategies.
Collects, prepares, processes, ships, and maintains inventory of research specimens.
Trains in developing protocol-specific systems and documents including process flows, training manuals, Standard Operating Procedures (SOPs) and Case Report Forms (CRFs).
Conducts and documents visits and testing/interviews according to all assigned regulatory and organizational protocols.
Trains in completing and submitting AE reports, according to institution and sponsor-specific reporting requirements.
Assists with the development of proposals or protocols as directed.
Identifies and communicates related shortcomings.
Maintains appropriate related documentation and tracks IP compliance at both protocol and subject level.
Maintains compliance with institutional requirements and policies.
Develops and maintains a familiarity with the ethical conduct of research and safeguards needed when conducting clinical research.
Trains in the design of safeguards to ensure ethical conduct and to protect vulnerable populations and participates in sponsor required training.
Trains on professional guidelines and code of ethics.
Proactively includes others in decision making and escalates issues to leadership as necessary.
Learns various stakeholders (statistical, operational, etc.) to ensure adequate design, implementation, and testing of clinical research program and/or study aims.
Investigates incomplete, inaccurate, or missing data/documents to ensure accuracy and completeness of data.
Recognizes and reports vulnerabilities related to security of physical and electronic data.
Assists with recognizing trends related to data quality and escalates as appropriate.
Adheres to and participates in the development and assessment of quality assurance.
Assists with identifying issues related to operational efficiency and shares results with team members.