Research Assistant I Roslindale Per Diem

Job Description:

I. Position Summary

Under the supervision of the Principal Investigator, the Research Assistant I supports research activities, including data collection, data management, clinical note review and annotation, and preparation of research materials. Responsibilities include reviewing Hebrew SeniorLife (HSL) clinical notes and systematically identifying and labeling information according to study-specific annotation guidelines.

The Research Assistant works collaboratively with investigators and research staff to maintain accurate, consistent research data and support project objectives.

II. Core Competencies

Results Orientation: Focuses on delivering superior performance by setting and achieving stretch goals.

Customer Service Orientation: Takes personal responsibility for understanding the real and underlying needs of customers’ and anticipating and meeting their expectations to establish viable, long-term relationships.

Teamwork and Collaboration: Works effectively within a team, group and across the organization and accomplishes tasks and desired results while behaving constructively as opposed to separately and competitively.

III. Position Responsibilities

Supports research activities across assigned projects, including data collection, data entry, database maintenance, and preparation of study materials.

Reviews and annotates HSL clinical notes using standardized, study-specific guidelines to identify and label clinical information relevant to research objectives.

Completes annotation training and calibration exercises; applies established annotation criteria consistently and refers ambiguous or complex cases to designated study personnel.

Performs quality assurance checks on annotated notes and research datasets, documents discrepancies, and participates in resolving annotation disagreements.

Maintains organized records of annotation decisions, study procedures, and project progress.

Assists with preparing research protocols, technical reports, summaries, and quantitative analyses under supervision.

Maintains familiarity with scientific literature relevant to assigned projects.

Protects the confidentiality of patient information and follows institutional requirements and study protocols for accessing, handling, and storing research data.

Participates in research team meetings and completes other duties consistent with the position as assigned.

IV. Qualifications

B.S. degree in scientific discipline, 2-3 years of related laboratory experience.

Must be professional, proactive, collaborative, conscientious and results-oriented individual.  Must have an optimistic and positive demeanor, excellent oral and written communication skills, good intuition and able to adapt to changing priorities and display good, sound judgment with a sense of humor.

Strong attention to detail and ability to apply standardized guidelines consistently.

Ability to review narrative clinical documentation, accurately extract relevant information, and recognize when clarification or supervisory review is needed.

Familiarity with medical terminology and clinical documentation preferred; study-specific training will be provided.

Experience with data entry, databases, electronic health records, or annotation tools preferred.

V. Physical Requirements

On file with Occupational Health

Remote Type:

Hybrid