About The Position

The Research Assistant II (RA2) will participate in multiple clinical studies as approved by the grant(s). The RA2 will oversee the administrative aspects of the grant and interact with study subjects, clinical research coordinators, study investigators, work study students and other research staff. Duties include but are not limited to, assisting with patient recruitment, scheduling study visits, administering questionnaires, creating and filing case report forms, entering and updating data, maintaining databases, running reports, storing samples, and performing other administrative tasks in support of the clinical studies. The RA2 maintains contact with the participating sites to insure complete and timely data collection, maintains patient profiles, assists with documenting financial and budgetary needs of the grant, and supporting the research team with the preparation of data and other reports.

Requirements

  • A minimum of a Bachelor’s degree is required.
  • At least one year relevant experience required. With Masters degree no experience required.
  • Experience with recruiting subjects, with an understanding of the ethical and technical conduct of research.
  • Excellent English communication skills (oral and written).
  • Cultural sensitivity and comfort with a wide range of social, racial and ethnic populations
  • Organizational ability to perform multiple tasks efficiently and to prioritize duties.
  • Proficiency with Microsoft Office applications including Word, Excel, and Access and PowerPoint.
  • Ability to perform basic data management tasks (coding, data entry, data cleaning, retrieval).
  • Ability to perform basic data analysis and reporting (in words, numbers and graphics).

Nice To Haves

  • Bilingual or multi-lingual skills (beyond that of English) appropriate to the patient population served is a plus.
  • Experience with statistical analysis tools a plus.
  • Experience using quantitative data analysis software helpful (e.g., SPSS, SAS, Minitab).

Responsibilities

  • Responsible for the administrative aspects of the research study, including: managing program records and handling communication needs of the program.
  • Provides assistance in the development of reports, presentations, and data analysis.
  • Assists in data collection and provides feedback on study’s progress.
  • Recruits subjects to participate in the study by using approved methodologies, such as, reaching to healthcare providers for referrals, visiting clinics, sending mailouts, using approved advertisements, etc.
  • Conducts the enrollment of study participants, including explaining research procedures, and obtaining informed consent of subjects and/or their families.
  • Schedules appointments of study participants; conducts reminder phone calls and/or sends mailouts.
  • Reviews the data collection forms for each enrollee for completion and quality; checks work of junior staff performing data entry to ensure timely and accurate entry.
  • Provides technical guidance to junior staff.
  • Obtains and distributes payment vouchers for participant reimbursements/participation.
  • Perform administrative duties associated with the study’s Data Monitoring and Safety Board, tracking and reporting adverse events and collecting data specified by the DSMB.
  • Responsible for all other administrative duties related to research activities.
  • Prepares and maintains Institutional Review Board (IRB) approvals and correspondence, including amendments and renewals as necessary.
  • Conducts literature searches.
  • Assists Investigators with manuscript and presentation preparation and research.
  • Participates in staff meetings/initiatives including appropriate quality improvement and education activities, or if unable to attend non-mandatory activities, accepts responsibility to review meeting minutes and becomes knowledgeable of issues discussed.
  • Performs office-related duties such as answering phones, picking up and delivering mail, ordering and distributing office supplies, handling faxes, scanning, filing, photocopying, collating materials, maintaining the update of policy manuals, etc.

Benefits

  • Competitive pay
  • Tuition reimbursement and tuition remission programs
  • Highly subsidized medical, dental, and vision insurance options
  • Career Advancement/Professional Development: Access a wealth of ongoing training and development opportunities that will not only enhance your skills but also expand your knowledge base especially for individuals pursuing careers in medicine or biomedical research.
  • Pioneering Research: Engage in groundbreaking research projects that are driving the forefront of biomedical science.
  • Flexible Spending Accounts
  • 403(b) savings matches
  • paid time off
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