Research Assistant II (Lab) (3772)

Posted Yesterday
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02446, Brookline, MA, USA
In-Office
26-30 Hourly
Junior
Healthtech • Professional Services • Biotech • Pharmaceutical
The Role
Supports clinical research by assisting with prescreening and patient visits, collecting and recording data in EDC/IVRS, performing phlebotomy and EKGs, managing samples and regulatory binders, completing sponsor and GCP training, and assisting with adverse event reporting and monitoring.
Summary Generated by Built In

The Research Assistant II (Lab) will be responsible for assisting the clinical research staff in conducting clinical research trials and assisting in the pre-screening process.


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.

KNOWLEDGE & EXPERIENCE


Education:

  • High school diploma or equivalent required

Experience:

  • 1-2+ years experience in the clinical field

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
  • Patient-centric focus.
  • Strong organizational and time-management skills.
  • Able to work in a fast-paced environment ensuring limited oversights.

Skills Required

  • High school diploma or equivalent
  • 1-2+ years experience in the clinical field
  • Phlebotomist certificate
  • Medical Assistant Certification
  • Knowledge of medical terminology
  • Ability to assist with blood drawing and lab processing
  • Ability to conduct EKG/ECGs
  • Able to manually take patient blood pressure
  • Excellent computer skills (experience with EDC/IVRS preferred)
  • Detail-oriented with strong organizational and time-management skills
  • Excellent customer service and patient-centric focus
  • Completion of GCP and IATA training and Sponsor-required protocol training
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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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