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Full-time

Clinical Research Associate

$62K/yr – $92K/yr

New Haven, CTScience & PharmaceuticalPosted 18d ago

You'll complete your application on the employer's website.

Role overview

Job type

Full-time

Salary

$62K/yr – $92K/yr

Posted

18 days ago

Job description

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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