Clinical Research Assistant I Job at Joule

Joule New Haven, CT 06511

Title: Clinical Research Assistant 1
Location: New Haven, CT
Duration: Direct Hire
Schedule: M-F 37.5 hours
Target Start Date: January 2023

Responsibilities:
The Clinical Research Assistant (CRA) will provide administrative support related to the collection and reporting of study-related clinical data. Responsibilities include, but are not limited to, with abstracting, assembling and organizing clinical research data, providing support in the compiling of patient scheduling, and assisting with reporting requirements.
  • Researches and collects data through site or home visit intakes; library research; structured interviews; or through other means for designated research assignments.
  • Records and compiles information related to research data. Codes data accordingly to research specifications. Uses a computer terminal to input and retrieve data and to generate reports.
  • Processes and summarizes data using scientific or statistical techniques. Assists in data interpretation and analyses. Reports on status of research activities.
  • Recruits and ensures that subject recruitment and follow-up are completed per protocol procedures.
  • Orders and maintains inventory of supplies. May assist in designing, developing, and modifying research experiments, procedures, or survey instruments. May assist research and support staff.
  • Performs additional functions incidental to research activities.
Requirements:
  • Six years of related work experience, four of them in the same job family at the next lower level, and high school level education; or four years of related work experience and an Associate's degree; or little or no work experience and a
  • Bachelor's degree in a related field; or an equivalent combination of experience and education.
  • Ability to work well in a clinical or research environment. Ability with medical terminology.
  • Proven ability to multi-task, maintain confidentiality and remain focused in a fast-paced environment. Proven ability to be meticulous with details.
  • Impeccable interpersonal skills and the ability to work as part of a team and independently. Professional appearance and manner as well as an excellent attendance record.
  • Ability to interact with all levels of clinical staff and study participants. Proven ability to communicate effectively, both verbal and written.
  • Intermediate to advanced computer proficiency with MS Excel and Word.


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