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SRI International
Plymouth, MI | Intern
$70k-92k (estimate)
2 Months Ago
Clinical Trials Intern
SRI International Plymouth, MI
$70k-92k (estimate)
Intern | Scientific Services 2 Months Ago
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SRI International is Hiring a Clinical Trials Intern Near Plymouth, MI

Overview

SRI’s Biosciences Division develops transformative approaches and platforms for challenging therapeutic problems. We conduct basic and translational research, have the breadth — and depth — to deliver the latest in biomedical research through technology development. Our researchers have a rich legacy of collaboration with government agencies and industry partners that improve health outcomes and well-being around the world. SRI Biosciences projects range from high-impact, early-stage research to drug co-development with pharmaceutical and biotech companies.

SRI's Clinical Trials Unit is current hiring for a summer intern. The intern will be exposed to a diverse range of responsibilities and will have the opportunity to work closely with experienced professionals in the field. This internship is designed to provide valuable insight and practical experience in clinical research while contributing to meaningful projects that have a direct impact on patient care and medical advancements. The Clinical Trials Intern will have the opportunity to gain hands-on experience across various facets of clinical research, including administrative, regulatory, clinical, laboratory, data management, and special projects. 

This position will work on-site in our Plymouth, MI office.

Responsibilities

  • Administrative Support:
    • Assist in organizing and maintaining research documents, including protocols, consent forms, and study materials.
    • Coordinate meetings, schedule appointments, and manage calendars for research team members.
    • Handle correspondence and communications with study participants, sponsors, and regulatory authorities.
  • Regulatory Compliance:
    • Assist in preparing and submitting regulatory documents for institutional review board (IRB) approval.
    • Maintain compliance with regulatory requirements and ensure adherence to study protocols and Good Clinical Practice (GCP) guidelines.
    • Track regulatory submissions and maintain up-to-date regulatory files.
  • Clinical Assistance:
    • Participate in the recruitment and screening of study participants.
    • Assist in the coordination of study visits and procedures, ensuring adherence to protocols and regulatory requirements.
    • Collect and record clinical data accurately and confidentially.
  • Laboratory Support:
    • Assist in laboratory procedures, sample processing, and storage as per study protocols.
    • Maintain laboratory equipment and supplies inventory.
    • Ensure compliance with laboratory safety protocols and procedures.
  • Data Management:
    • Assist in data collection, entry, and validation using electronic data capture (EDC) systems.
    • Perform quality control checks on collected data and assist in data cleaning and analysis.
    • Generate reports and summaries of study data for analysis and presentation.
  • Special Projects:
    • Contribute to additional special projects as needed, such as literature reviews, protocol development, or process improvement initiatives.
    • Collaborate with team members to accomplish project objectives within specified timelines. 
  • Qualifications

    • Currently enrolled in a Bachelor's or Master's degree program in a relevant field (e.g., biology, clinical research, public health, nursing, or related discipline).
    • Proficiency in Microsoft Office suite (Word, Excel, PowerPoint).
    • Familiarity with clinical research concepts and regulatory requirements preferred.
    • Ability to work independently and collaboratively in a fast-paced environment.
    • Detail-oriented, quick learner who pays attention to detail and has good organization skills.
    • Excellent written and verbal communication skills.

    The salary range is: $22-$30/hr. Salary ranges will vary and are based on several factors, including geographic location, market competitiveness and equity amongst internal employees in similar roles. Positions may also qualify for SRI's Pay for Outstanding Performance program or the annual Performance Based Compensation program. SRI also has a competitive benefits package, to view details please go to https://www.sri.com/resources/benefits/.

    SRI is an independent nonprofit research institute headquartered in Menlo Park, Calif., with a rich history of supporting government and industry. We create and deliver world-changing solutions for a safer, healthier, and more sustainable future. For more than 75 years, we have collaborated across technical and scientific disciplines to discover and develop groundbreaking?products and technologies and bring innovations and ideas to the marketplace.

    Job Summary

    JOB TYPE

    Intern

    INDUSTRY

    Scientific Services

    SALARY

    $70k-92k (estimate)

    POST DATE

    03/30/2024

    EXPIRATION DATE

    05/01/2024

    WEBSITE

    sri.com

    HEADQUARTERS

    MENLO PARK, CA

    SIZE

    1,000 - 3,000

    FOUNDED

    1946

    TYPE

    NGO/NPO/NFP/Organization/Association

    CEO

    WILLIAM JEFFREY

    REVENUE

    $200M - $500M

    INDUSTRY

    Scientific Services

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    About SRI International

    SRI International provides basic and applied research, laboratory and advisory services.

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