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  3. Research Assistant II (Non-Lab) (3773)
Job detail

Research Assistant II (Non-Lab) (3773)

DM CLINICAL RESEARCH GROUP

Employer page
#Phlebotomy#Medical Terminology#FDA Regulations#Medical Assistant#SOPs#Clinical Research#GCP#EKG#Clinical Trials
#ECG
#IATA
#IRB
OtherOn Site0-2 yrs$24 - $28 / HOURPosted 3 days agoCloses Jul 27

Location

New York

Salary

$24 - $28 / HOUR

Quick overview

Assist clinical research staff in conducting trials, pre-screening patients, and collecting data via EDC systems. Perform clinical tasks including blood draws, EKG/ECGs, and maintaining regulatory binders.

Requirements summary

Requires a high school diploma and 1-2+ years of experience in the clinical field. Phlebotomist or Medical Assistant certifications are preferred, along with knowledge of medical terminology.

high schoolprofessional certificateTime ManagementPhlebotomyMedical TerminologyClinical ResearchRegulatory DocumentationPatient ScreeningFDA RegulationsPatient Data CollectionBlood Pressure MonitoringEDC SystemsGCP/ICH GuidelinesEKG/ECG

Job description

Job DetailsJob Location

  • Brooklyn,
  • NY (AOM) -
  • Brooklyn,
  • NY 11220Salary
  • Range: $24.00 - $28.00 HourlyThe Research Assistant II (Non 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

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DM CLINICAL RESEARCH GROUP

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Hiring organization

DM CLINICAL RESEARCH GROUP

DM Clinical Research is a network of clinical trial investigator sites with headquarters based out of Houston, Texas. We are the link connecting pharmaceutical and research organizations to caring individuals seeking to power the advancement of medicine. We work with qualified...

Explore employer profile
IndustryBiotechnology Research
TypePrivately Held
Size501-1,000 employees
HQHouston, TX
Founded2006
  • 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. Qualifications
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