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Research Assistant - Flowood, MS

Iterative Scopes

Flowood, MSFull-timeNo compensation foundPosted 2mo agoVerified open 5 days ago

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At a glance

Compensation
No compensation found
Location
Flowood, MS
Schedule
Full-time
Work Authorization
Not specified

Job overview

Iterative Scopes is hiring a Research Assistant - Flowood, MS. The Research Assistant (RA) is a specialized research professional who works under the direction of the Clinical Principal Investigator (PI) and site management. The RA's primary responsibility is to assist Clinical Research Coordinators with conducting research studies, supporting and facilitating daily clinical trial activities, and playing a supportive role in study conduct.

Key focus areas include Assist Study Team with communicating study requirements to all individuals involved in the study, Work with the Study Team to develop and implement recruitment strategies, and Assist Study Team with screening subjects for eligibility.

Successful candidates bring High School Diploma Or Equivalent, 2+ Years Healthcare Experience, and Must Be Able To Lift Up To 25 Pounds. Important skills include Strong Written Communication Skills, Strong Verbal Communication Skills, Ability To Read, Interpret, And Apply Clinic Policies, Ability To Read, Interpret, And Apply Research Protocols, and Standard Office Software. Preferred (not required): Communicating Study Requirements, Develop Recruitment Strategies, Implement Recruitment Strategies, and Screening Subjects For Eligibility.

Skills & qualifications

RequiredNice to have

Skills

Strong Written Communication SkillsStrong Verbal Communication SkillsAbility to Read, Interpret, and Apply Clinic PoliciesAbility to Read, Interpret, and Apply Research ProtocolsStandard Office SoftwareCommunicating Study RequirementsDevelop Recruitment StrategiesImplement Recruitment StrategiesScreening Subjects for EligibilityDocumenting Eligibility or ExclusionRegister Participants in Clinical Trial Management SystemMaintain Inventory of Study SuppliesInvestigational Drug/Device AccountabilityCompleting Study DocumentationMaintenance of Study FilesMaintaining Effective and Ongoing CommunicationManage Day to Day ActivitiesProblem SolvingProtocol ManagementCollect and Report Patient Recruitment/Enrollment Progress and MetricsProcess and Ship SpecimensIATA RegulationsArranges Secure Storage of Study DocumentsGood Clinical Practice GuidelinesEnter Patient Visit Data in E-CRFProtection of Rights and Welfare of Human Research ParticipantsCooperate With Site Compliance and Monitoring EffortsAccess, Use, and Disclosure of PHIPerform Quality WorkInteract ProfessionallyWork Effectively as a Team ContributorWork Independently

Qualifications

High School Diploma or Equivalent2 Years in a Healthcare SettingAbility to Lift Up to 25 PoundsSome College

Full job description

Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes.

We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need. Today, Iterative Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees world-wide.

We are seeking a full-time, on-site Research Assistant (RA). The RA is a specialized research professional working with and under the direction of the Clinical Principal Investigator (PI) and site management. The primary responsibility of the RA is to assist the Clinical Research Coordinators with conduct of research studies. The RA supports and facilitates the daily clinical trial activities and plays a supportive role in the conduct of the study.

Responsibilities

  • Assists Study Team with communicating study requirements to all individuals involved in the study
  • Works with the Study Team to develop and implement recruitment strategies in accordance with site policies and IRB requirements and approvals
  • Assists Study Team with screening subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant’s eligibility or exclusion
  • Assists Study Team as requested to register participants in the Clinical Trial Management System to ensure billing of study procedures to appropriate funding source
  • Maintains inventory of study supplies. If handling investigational drugs/devices, follows the sponsor protocol and/or site policies on Investigational Drug/Device Accountability
  • Assists Study Team in completing study documentation and maintenance of study files in accordance with sponsor requirements and site policies and procedures including, but not limited to, consent forms, source documentation, narrative notes if applicable, case report forms, and investigational material accountability forms
  • Aids the Study Team in maintaining effective and ongoing communication with sponsor, research participants, site management and PI during the course of the study
  • Works with the Study Team to manage the day to day activities of the study including problem solving, communication and protocol management
  • Collects and reports ongoing patient recruitment/ enrollment progress and metrics to site management and PI
  • As directed, process and ship specimens per study protocol and IATA regulations
  • Arranges secure storage of study documents that will be maintained according to Good Clinical Practice guidelines or for the contracted length of time, whichever is longer
  • Enter all patient visit data in e-CRF and CTMS on a daily basis or as directed
  • Assists Study Team in protection of the rights and welfare of all human research participants involved in research in accordance with Federal regulations
  • Cooperates with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance
  • Other duties as assigned Iterative Health Expectations

All employees are expected to:

  • Perform quality work within deadlines with or without direct supervision

  • Interact professionally with other employees, customers and suppliers

  • Work effectively as a team contributor on all assignments

  • Work independently while understanding the necessity for communicating and coordinating work efforts with other employees and organizations Qualifications

  • High school diploma or equivalent. Some college preferred

  • Minimum 2 years in a healthcare setting

  • Strong written and verbal communication skils

  • Ability to read, interpret, and apply clinic policies and research protocols

  • Ability to use standard office software

  • Must be able to lift up to 25 pounds At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact [email protected].

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