Research Assistant, Cpc - Nutley, United States - Hackensack Meridian Health

Hackensack Meridian Health

Verified Company

Nutley, United States

3 weeks ago

Posted by:

Mark Lane

beBee recruiter

Description

Overview:

The
Research Assistant, CPC will be responsible for the day-to-day completion of tasks necessary for the success of an assigned behavioral science research project or set of related projects performed by or in conjunction with the Cancer Prevention and Control Program of Hackensack University Medical Center/John Theurer Cancer Center.

The **Center for Discovery and Innovation

CDI
was established by
Hackensack Meridian _Health_** (HMH) as an academic basic and translational research enterprise to rapidly translate science innovation to the clinic and to improve outcomes for patients with cancer, infectious diseases, autoimmune disease and other acute and chronic diseases. The CDI has grown rapidly since its origins in 2019, and now has 32 labs, 190 scientists and allied personnel supported by 60 NIH grants and more than 30 other grants and contracts. Areas of expertise include genomics, epigenetics, drug resistance, stem cell biology, drug discovery, diagnostics and biomarker development, and pharmacology.

Responsibilities:

A day in the life of a
Research Assistant, CPC at Hackensack Meridian _Health_ includes:

Identifies potential participants, schedules screening and enrollment, obtains consent, administers measurement protocols, and completes activities related to ensuring participant retention, with oversight.
Assists with administrative aspects of coordinating activities with other funded sites.
Monitors wellbeing of research participants through measures and interactions with participants, notifying study staff of participants who appear to be impaired or distressed so that proper steps can be taken.
Assists with entering and managing data, performing routine data quality assurance procedures, and helping resolve discrepancies, with oversight.
Performs background research for manuscripts, publications, and research projects.
Maintain bibliographies and a database of important articles and manuscripts.
Assists in preparing and organizing study records, scheduling meetings, preparing and distributing meeting minutes.
Assists with payment, tracking, and documentation of patient study incentives.
Assists with IRB approvals and paperwork.
Other administrative tasks as assigned.

Qualifications:

Education, Knowledge, Skills and Abilities Required:

Bachelor's degree in a related field or equivalent years of experience.
Excellent oral and written communication skills.
Ability to make good administrative/procedural decisions and judgments.
Ability to work independently to plan, organize and prioritize multiple tasks.
Knowledge of research methods and topical content of assigned study.
Ability to deal effectively and professionally with persons ranging from leaders of national organizations, senior faculty, fellow RAs and patients.