Research Assistant I (Lab) (4170)

Posted 3 Days Ago
Be an Early Applicant
77375, Tomball, TX, USA
In-Office
Entry level
Healthtech • Professional Services • Biotech • Pharmaceutical
The Role
Assists clinical research staff with clinical trial activities, including patient visits, data collection, specimen handling and shipment, regulatory documentation, protocol training, source document creation, adverse event reporting, and audit or monitoring issue resolution. Maintains accurate study records and follows FDA regulations, GCP/ICH guidelines, sponsor requirements, organizational SOPs, and study protocols.
Summary Generated by Built In

The Research Assistant I (Lab) 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.
  • Any other matters as assigned by management.

KNOWLEDGE & EXPERIENCE

Education:

  • High school diploma or equivalent required

Experience:

  • Prior experience in clinical research is not required but preferred

Credentials:

  • Phlebotomist certificate preferred
  • Medical Assistant 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

Skills Required

  • High school diploma or equivalent
  • Prior clinical research experience
  • Phlebotomist certificate
  • Medical Assistant Certification
  • Knowledge of medical terminology
  • Detail-oriented with strong attention to detail
  • Excellent customer service skills
  • Excellent computer skills
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The Company
700 Employees
Year Founded: 2006

What We Do

DM Clinical Research is a multi-therapeutic network of clinical trial investigator sites headquartered in Houston, Texas. Founded in 2006, the company connects patients with trusted physicians to conduct cutting-edge research focused on quality and compassion, aiming to deliver advanced, preventative medicine to underserved communities. They operate a national network of dedicated research centers and physician-embedded sites throughout the United States.

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