Clinical Research Assistant

MedStar Health; Washington (District of Columbia); On-site; USD 26,000 - 45,000; Full time

Job summary

MedStar Health in Washington, DC seeks a Clinical Research Assistant to support departmental clinical research efforts, entering study data into CTMS and ensuring data quality. The role involves on-site coordination of participant visits, handling biospecimens, and supporting sponsor visits, with emphasis on timely data entry and regulatory compliance.

You will work under supervision to assist the clinical research team, manage multiple tasks, and uphold data integrity in a fast-paced

Qualifications

• High School Diploma or GED is required.
• Associate's degree or allied health professional degree preferred.
• 2 years of related field experience preferred.
• Experience managing multiple priorities preferred.
• Verbal and written communication skills are required.
• Basic computer skills preferred.

Responsibilities

• Assists IRB submissions and delegation of authority as applicable.
• On-site support of scheduling research participant visits and reminders.
• Update and maintain data entry into CRFs and CTMS within one business day.
• Record ancillary service reports and complete required clinical trial data fields.
• Collects and ships biospecimens per protocol and maintains OSHA training.
• Maintain IATA training for transport of biological materials; manage lab supplies.

Skills

Verbal and written communication

Basic computer skills

Education

High School Diploma or GED

Associate's degree

Job description

About the Job

General Summary of Position

Under the direct supervision of the Manager the Clinical Research Assistant will support the facilitation and conduct of departmental clinical research efforts and support the clinical research team by performing a variety of research database and administrative duties in support of clinical trials to ensure adherence to protocols and quality of information received. Required to enter study and/or research participant data into the Clinical Trial Management System (CTMS) as applicable.

Primary Duties and Responsibilities

• Assists the clinical research team with Institutional Review Board (IRB) submissions as applicable; ensures the appropriate delegation of study related tasks (i.e. Delegation of Authority).
• On-site support of scheduling research participant visits; calls or sends reminders to research participants for scheduled visits.
• Accurately updates and maintains data entries into case report forms (CRFs) and the Clinical Trial Management System (CTMS) within one (1) business day; incorporate applicable source documents (e.g. surgical reports pathology reports medical history).
• Obtains and records ancillary service reports (e.g. x-ray pathology ECG laboratory); completes all required clinical trial data fields as applicable and addresses all queries and clarifications; upholds data integrity in a high-quality reliable and statically sound manner; completes and submits case report forms on as close to a real time basis as possible.
• Collects processes and ships biospecimens and/or materials as applicable and according to each protocol; maintains current Occupational Safety and Health Administration (OSHA) training regarding Bloodborne Pathogens.
• Maintains International Air and Transportation Association (IATA) training for routine packaging labeling and transporting of biological materials; maintains supply inventory (e.g. lab kits) and provides general support to the clinical research team including ordering and distributing non-drug clinical trial supplies.
• Assists the clinical research team in the preparation and on-site support of sponsor visits; works effectively with multidisciplinary ancillary and inter-professional research teams; possesses a basic understanding of scientific center goals and the importance of serving our customers.

Minimal Qualifications

Education

• High School Diploma or GED required
• Associate's degree oran allied health professional degree preferred

Experience

• Prior work experience not required
• 2 years experience in related field preferred
• Experience managing multiple priorities preferred

Knowledge Skills and Abilities

• Verbal and written communication skills.
• Basic computer skills preferred.

This position has a hiring range of

USD $18.70 - USD $32.72 /Hr.