Clinical Trials Research Associate

1 week ago

Boston, Massachusetts, United States Mass General Brigham Full time

GENERAL SUMMARY/ OVERVIEW STATEMENT:

The Mass General Brigham team is at the forefront of advancing diagnostic methodologies for infectious diseases. We are currently seeking a dedicated and enthusiastic Clinical Research Coordinator to contribute significantly to our innovative projects. This role will involve engaging in various research initiatives focused on infectious diseases, particularly those related to sexually transmitted infections, respiratory pathogens, and vector-borne diseases. The selected candidate will collaborate closely with leading researchers to develop and assess new diagnostic tools for sexually transmitted infections in clinical settings.

The ideal applicant will hold a bachelor's degree (conferred or anticipated) and demonstrate a strong academic performance, exceptional interpersonal abilities, and a proactive approach to their work. A keen interest in pursuing a career in healthcare or scientific research is essential. Previous experience in clinical research, data management, and laboratory techniques is advantageous but not mandatory.

PRINCIPAL DUTIES AND RESPONSIBILITIES:

Project Coordination Responsibilities:

  • Recruiting participants for research studies and securing informed consent.
  • Managing study data utilizing REDCap (Research Electronic Data Capture) systems.
  • Assisting with additional data entry and management tasks.
  • Regularly liaising with principal investigators to ensure participant safety and compliance with study protocols.
  • Providing general administrative support as needed.
  • Collaborating on academic projects with principal investigators, including lectures and conference presentations.
  • Working alongside other research assistants and clinical research coordinators on various research endeavors.

Laboratory Responsibilities:

  • Labeling and analyzing samples collected from clinical settings.
  • Preparing and conducting routine experiments as instructed and analyzing results.
  • Maintaining a detailed laboratory notebook.
  • Preparing reagents, instruments, and materials for experiments.
  • Assisting in organizing materials for publication or presentation.
  • Managing and ordering laboratory supplies.

SKILLS/ABILITIES/COMPETENCIES REQUIRED:

  • Strong interpersonal skills and the ability to function effectively within a diverse team.
  • Comfort in engaging with study participants.
  • Capability to work independently, demonstrate initiative, and prioritize responsibilities.
  • Excellent written and verbal communication skills.
  • Outstanding organizational abilities and capacity to manage multiple tasks simultaneously.
  • Keen attention to detail and proficiency in documenting research activities.
  • Familiarity with Microsoft Office Suite (Word, PowerPoint, Outlook).
  • Ability to follow detailed instructions.
  • Basic understanding of clinical research protocols.
  • Commitment to respecting and upholding the rights and needs of study participants.

EDUCATION:

  • A bachelor's degree is required, with coursework in biology, psychology, public health, pre-medical sciences, or related fields preferred.

EXPERIENCE:

  • Recent graduates with relevant coursework or project experience will be considered for entry-level positions.
  • Candidates with 1-2 years of relevant work experience may be considered for more advanced roles.

SUPERVISORY RESPONSIBILITY:

  • Entry-level positions do not entail supervisory duties.
  • More experienced coordinators may assist in training new staff members.

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