Clinical Research Assistant - Washington, United States - Children's National Hospital

Children's National Hospital

Verified Company

Washington, United States

2 weeks ago

Posted by:

Mark Lane

beBee recruiter

Description

Description

The Clinical Research Assistant performs a variety of research, data and clerical duties of a routine and technical nature to support the conduct of clinical research under the direction of a senior research team member.

The Research Assistant will develop a progressive functional knowledge of Good Clinical Practices (GCP), Office of Human Research Protections (OHRP) regulations and Food and Drug Administration (FDA) regulations.

In this role, the Clinical Research Assistant completes tasks including identifying eligible participants under the supervision of a senior research team member, preparing necessary documents, equipment, supplies, etc.

for research visits and conducting and documenting visits and protocol-specific testing/interviews according to study protocol, operational plans of clinical departments and Standard Operating Procedures (SOPs) for mínimal risk studies or for other studies.

The Addressing Disparities Through Advocacy, Prevention, and Technology (ADAPT) Research Lab led by Dr. Monika Goyal is looking for an enthusiastic and motivated individual for a clinical research assistant position. This position will provide support to several ongoing studies to address inequities in emergency department care.

Strong verbal and written communication skills
Organizational skills with attention to detail
Ability to work closely with a diverse team including stakeholders, investigators, and research staff
Commitment to improving healthcare delivery and outcomes

Qualifications

Minimum Education
Bachelor's Degree BA/BS degree in a science, technical, health-related field or another applicable
discipline. (required) Or

Minimum Work Experience
0 years Experience working in a medical or scientific research setting (preferred)

Functional Accountabilities

Responsible Conduct of Research

Consistently demonstrates adherence to the standards for the responsible conduct of research.
Plans, conducts and manages research projects within federal and institutional regulations and policies under the direction of the principal investigator.
Uses research funds and resources appropriately.
Maintains confidentiality of data as required.
Meets all annual jobrelated training and compliance requirements.

Research Administration

Maintains knowledge and comprehension of assigned research protocols, including study procedures, timelines and eligibility.
Accurately creates, completes, maintains and organizes study documents.
Accounts for study materials, including participant lists and visit logs, regulatory binders, case report forms, laboratory kits, investigational product(s) and participation incentives.
Attends study meetings, which could include overnight travel, as requested by principal investigator.
Works well with other members of the research team and seeks and provides input when appropriate.

Participant Enrollment

Adheres to the IRBapproved recruitment plan.
Identifies participants that meet eligibility requirements under the supervision of a senior research team member.
Interacts with study participants and/or legally authorized representatives (LARs) to communicate study purpose and participation details and to assess participation interest.
Engages participants/LARs in the informed consent process according to institutional policies.
Follows procedures for documenting participant incentive distribution.

Study Management

Plans, conducts and manages research activities in accordance with federal regulations and guidance documents and sponsor and institutional policies under the direction of a senior study team member.
Conducts and documents visits and protocolspecific testing/interviews according to study protocol, operational plans of clinical departments and SOPs for mínimal risk studies or for other studies under direction.
Completes accurate IRB submissions within institutional timeframes.
Records participant visits in the appropriate tracking system.

Data Collection

Ensures data is collected as required by protocol and in accordance with research data principles (

ALCOAC:
Attributable, Legible, Contemporaneous, Original, Accurate and Complete).

Ensures that queries are resolved within sponsor and institutional timelines.
Plans and performs research specimen collection, labeling and storage/shipping if assigned; maintains accurate sample accountability/chain of custody documentation.
Ensures secure storage of study documents and assists in maintaining regulatory documents per sponsor and institutional requirements.
Anticipate and responds to customer needs; follows up until needs are met

Teamwork/Communication