Clinical Research Associate
$62K/yr – $92K/yr
You'll complete your application on the employer's website.
$62K/yr – $92K/yr
You'll complete your application on the employer's website.
Job type
Salary
$62K/yr – $92K/yr
Location
Sector
Posted
18 days ago
Yale University is hiring a Clinical Research Associate to implement clinical research operations in the Testani laboratory. The role supports heart failure studies through participant recruitment and consent, accurate data and regulatory management, study procedures, and biospecimen processing.
Responsibilities
Implementation of the clinical research operation of the Testani laboratory; will be responsible for working independently and in collaboration with the research team towards recruitment of participants for the research protocols, obtain informed consent, responsible for creation and, maintenance of accurate data records, managing of regulatory compliance in several ongoing heart failure studies in both hospitalized and ambulatory patients work in conjunction with the research team to carry out study procedures and process biospecimen
Recommends the design and implementation of procedures and protocols under the direction of a higher-level authority
Investigates, analyzes, and reaches preliminary scientific conclusions related to research planning
Ensures data results are compiled, analyzed, and presented properly
Analyzes, develops and interprets scientific results. Maintains clear documentation of results. Prepares scientific reports and papers for research proposals and published reports
Performs independent research and laboratory techniques and participates in experimental research planning
Interacts with internal contacts including the PI, research assistants, graduate students, Radiation Safety and Biological Safety officers, and Animal Care personnel to discuss and evaluate research results and to ensure the smooth and safe operation of the laboratory
Interacts with external contacts such as researchers at other institutions, staff at biotechnology and reagents companies to consult on research methods and to keep abreast of product information and developments
May perform other duties as assigned
Preferred
Master's degree in a related field and three years of related work experience in the same job family or an equivalent combination of experience and education
Knowledgeable in Redcap, Epic, OnCore, tele and video consenting and phlebotomy
Master's degree in a related field and three years of related work experience in the same job family or an equivalent combination of experience and education.
REDCap
Epic
OnCore
Teleconsenting
Video consenting
Phlebotomy
Benefits
Hybrid work model
Company
Research university focused on education and knowledge advancement
New Haven, Connecticut, USA
https://www.yale.edu/
Founded in 1701
10001+ employees
Qualifications
Strong organization skills, attention to detail and the ability to prioritize and multi-task
Prior experience with clinical trials, with demonstrated ability to function as a collaborative member of a clinical research team and communicate well with participants and providers
Demonstrated excellence in organizational skills, attention to detail, and ability to multi-task
Skilled in obtaining informed consent, proven skill for laboratory sample processing and collecting vital signs
Excellent time management skills to manage multiple ongoing projects
Excellent oral and written communication skills
Proven experience with IND studies and managing regulatory documents
Flexibility and willingness to learn new skills/adapt to different settings i.e. study specific requirements
Master's Degree in a scientific discipline and one year experience or an equivalent combination of education and experience
Master's degree in a related field and three years of related work experience in the same job family or an equivalent combination of experience and education
Knowledgeable in Redcap, Epic, OnCore, tele and video consenting and phlebotomy
Master’s Degree in a scientific discipline and one year experience or an equivalent combination of education and experience.
Required skills
Clinical Trials, Informed Consent, Laboratory Sample Processing, Vital Signs Collection, IND Studies, Regulatory Documents, REDCap, Epic, OnCore, Telephonic and Video Consent, Phlebotomy
Experience
1+ years
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