Research Associate Sr

Responsibilities

• Participate in the day to day activities research studies on women's health including an interventional clinical trial, including participant recruitment, screening, enrollment, and scheduling in accordance with protocol defined inclusion/exclusion criteria.
• Administer protocol adherent execution of all study procedures, including laboratory testing, ambulatory/wearable monitoring, training on electronic diaries, administration of behavioral and neurocognitive assessments, and other study evaluations.
• Process blood and related biological samples, including Venipuncture and blood collection from participants, preparation of study equipment and phlebotomy tubes, sample labeling, handling, storage, and transport to designated laboratories in compliance with protocol and safety requirements.
• Collaborate closely with investigators, study physician, study coordinator, pharmacists, laboratories, and other stakeholders to support efficient and compliant study execution.
• Mentor, train and assist with supervising junior research staff as needed.
• Enter study data into databases.
• Affiliate with preparation of scientific articles, IRB, and grant submissions as needed.
• Perform other duties as assigned.

Qualifications

• Master's Degree in Psychology, Neuroscience, Counseling, Sociology or related research field and 1 year of work experience in a research project and/or related clinical setting OR Bachelor's Degree in Psychology, Neuroscience, Counseling, Sociology or related research field and 3 years of work experience in a research project and/or related clinical setting.
• Familiarity with computers and common software packages required.
• Working knowledge of research methodology strongly preferred.