Adecco Job - 39211309 | CareerArc
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Company: Adecco
Location: Minnetonka, MN
Career Level: Mid-Senior Level
Industries: Recruitment Agency, Staffing, Job Board

Description

A Medical Lab Project Manager/Study Coordinator job in Minnetonka, MN is now available courtesy of Adecco Medical & Science. This is a contract position starting ASAP and going for approx. 6 months but could get extended based on business needs and could also be temp-hire for the ideal candidate.

The Research and Development team Query Lab seeks to advance innovation efforts and learnings to improve the ways we detect, intercept and prevent disease. We are looking for a Study Coordinator to work directly with study participants in this new research facilities. The Study Coordinator will support the design and implementation of studies while ensuring study participants' safety, privacy, data security, and satisfaction.

Job duties:

Study Preparation:

  • Organize space for study equipment and supplies.
  • Consult and provide feedback on research study sites and determine staff or equipment availability.
  • Participate in the development of study protocols including guidelines for administration or data collection procedures.
  • Review proposed study protocols to evaluate factors such as sample collection processes, data management plans, and potential subject risks.
  • Instruct research staff in scientific and procedural aspects of lab studies including standards of care, informed consent procedures, or documentation procedures.
  • Function as Electronic Data Capture (EDC) subject matter experts during study start-up, facilitating the design of each study in the EDC
  • Study Implementation:

  • Ensure participants are properly scheduled for appointments, procedures, or inpatient stays as required by study protocols.
  • Oversee subject enrollment to ensure that informed consent is properly obtained and documented.
    Inform and discuss with study participants study aspects and outcomes to be expected while participating in a study.
  • Perform specific protocol procedures such as interviewing subjects, taking vital signs, and performing electrocardiograms.
  • Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.
  • Track enrollment status of subjects and document dropout information such as dropout causes and subject contact efforts.
  • Direct the requisition, collection, labeling, storage, or shipment of specimens.
  • Communicate with lab team and/or research team regarding laboratory findings
  • Identify protocol problems, inform investigators of problems, or assist in problem resolution efforts such as protocol revisions.
  • Prepare study-related documentation such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, and progress reports.
  • Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.
  • Study Results:

  • Evaluate or interpret interim study data.
  • Collaborate with investigators to prepare presentations or reports of clinical study procedures, results, and conclusions.
  • Maintain required records of study activity including case report forms, drug dispensation records, or regulatory forms.
  • Partner with lab and research teams and coordinate site visits to analyze discrepancies and answer questions about issues such as incomplete data.
  • Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies.
  • Required Qualifications:

    • Bachelor's degree or equivalent education
    • 3+ years of research consulting experience including protocol review and study implementation
    • 3+ years' experience demonstrating critical thinking skills
    • 2+ years' experience successfully thriving in an environment with ambiguity
    • Proven ability to be organized, possess the ability to prioritize, take initiative and commit to the completion of each assigned project
    • High level of Microsoft Office proficiency
    Preferred Qualifications:
    • Experience using RedCap Clinical Management Software
    • Four-year degree within a science related field (e.g. biology)

    If you are interested in this job opportunity, then please click APPLY NOW. For other opportunities available at Adecco Medical and Science go to www.adeccousa.com.

    Equal Opportunity Employer/Veterans/Disabled. To read our Candidate Privacy Information Statement, which explains how we will use your information, please visit http://www.adeccousa.com/candidate-privacy/. The Company will consider qualified applicants with arrest and conviction records



    Equal Opportunity Employer/Veterans/Disabled

    To read our Candidate Privacy Information Statement, which explains how we will use your information, please

    The Company will consider qualified applicants with arrest and conviction records


     Apply on company website