Research Assistant III (3659)

Job DetailsJob Location: Sugarland - Sugar Land, TX 77478The Research Assistant III will be responsible for assisting the clinical research staff in conducting clinical research trials.

DUTIES & RESPONSIBILITIES

Completing DMCR-required training, including GCP and IATA.

Maintaining a working knowledge of current FDA regulations, GCP/ICH guidelines, organizational SOPs, guidance documents, and study protocols.

Assisting in the collection and recording of patient data per Sponsor requirements via the respective EDC system.

Timely and accurately assist in collection, management, and shipment of subjects' samples, and/or specimens

Completing Sponsor-required training prior to study-start, including, but not limited to

Sponsor-provided and IRB-approved protocol

All amendments

Investigator Brochure

Sponsor-specified EDC and/or IVRS

This includes completing the above-mentioned training prior to any study-related procedures being conducted on that said protocol should the RA be added to a protocol post-study start.

Maintaining clear, concise, accurate, and legible records.

Being prepared for and available at all required company meetings and monitoring visits for their assigned protocols at their respective site(s).

Utilizing the most recent version of the Protocol, Informed Consent, and Investigator Brochures at their respective site(s).

Assisting in the compilation and organization of all regulatory and administrative binders for their assigned protocols at their respective site(s) upon initial receipt of and wherever applicable.

Assisting in the creation of source documents for their assigned protocols at their respective site(s).

Conducting patient visits.

Assisting in reporting Adverse and Serious Adverse Events to the appropriate authorities per Sponsor.

Assisting in addressing and resolving issues from internal/external audits and monitoring letters for all assigned protocols at their respective site(s) in a timely manner.

Assists with all other aspects of the study and conducts as needed.

Assist the lab team in conducting EKG/ECGs.

Assist the lab team in blood drawing and lab processing.

Able to manually take patient blood pressure.

Assists in conducting rapid clinical tests.

Any other matters as assigned by management.

Oversee all of the Research Assistant(s) workflow ensuring all projects and tasks are completed efficiently, accurately, and effectively.

Assist coordinators with pre-screening basics and assist with administering patient IVs.

Any other matters as assigned by management.

KNOWLEDGE & EXPERIENCE

Education:

High school diploma or equivalent, required

Bachelor’s Degree in a medical field or Foreign Medical Graduate, required

Experience:

3+ years in the clinical field, required

Credentials:

Phlebotomist certificate, preferred

Medical Assistant Certification, preferred

IV Administration Certification, preferred

Knowledge & Skills:

Knowledge of medical terminology required

Must be detail-oriented and demonstrate attention to detail

Excellent customer service skills

Excellent computer skills

Ability to manage multiple projects at a time.

Qualifications