Clinical Research Assistant

Actalent•Hollywood, FL

40d•$35,360 - $47,840•Onsite

About The Position

The Research Assistant provides direct support to Clinical Research Coordinators to achieve protocol-specific study goals, ensuring strict adherence to ICH, GCP, protocol, and site guidelines and policies. This role is integral in facilitating the smooth operation of clinical research activities.

Requirements

Bachelors degree in Biology, Psychology, or related
Ability to thrive in a fast-paced environment and multitask effectively.
Proficiency in Microsoft Word and Excel.
Strong interpersonal skills and ability to communicate clearly both orally and verbally.

Nice To Haves

Interest in and knowledge of specific study indications
Excellent computer skills and advanced knowledge of electronic equipment
Skilled in organization and record maintenance
Ability to develop and maintain effective working relationships with supervisors and coworkers
Strong personal initiative and attention to detail
Ability to react calmly and effectively in emergency situations
Ability to interpret, adapt, and apply guidelines and procedures
Bilingual in Spanish

Responsibilities

Serve as the Clinical Research Coordinator's right hand in various tasks, including seeing patients and preparing lab kits and patient binders.
Assist with enrollment logs and other study-related documentation as needed.
Create and maintain patient charts for all assigned studies.
Prepare participant visits based on the Clinical Research Coordinator's schedule, ensuring all source documents, assessments, lab kits, and other visit materials are available and accurate.
File lab results, EKG results, and other communication in designated patient charts.
Maintain inventory of study-specific supplies, including lab kits, assessments, and participant-facing materials.
Complete data entry and query resolution for all Case Report Forms (CRFs) in a timely manner, based on sponsor-specific timelines and deadlines.
Assist Coordinators in assessments, including but not limited to blood pressure and urine collection.
Communicate with study participants, caregivers, third-party vendors, and laboratories as needed.
Assist Coordinators with scheduling, copying, faxing, and other clerical tasks.
Aid Coordinators in the facilitation of study monitoring visits.
Complete daily responsibilities delegated by the Clinical Research Coordinator as they pertain to the study and/or participants.
Assume other duties and responsibilities as assigned.