• Clinical Supply Associate - Packaging - 2nd Shift

    Job Locations - | US-PA
    Posted Date 2 months ago(2 months ago)
  • Overview

    Do you want to be responsible for packaging and labeling duties per standard operating procedures within Clinical Supplies



    Who are we?

    We Are PRA.


    We are 15,000+ employees strong, operating in more than 85 countries. We are committed to saving lives, and we are constantly striving to be the best at what we do. Our impact is real and we see it every single day. We are getting live saving drugs into the hands those who need them most.


    Who Are You?


    You are an experience professional with a passion for clinical supplies. You are organized, but flexible and adaptable to unexpected changes. You can easily envision the bigger picture, without losing sight of the day-to-day tasks. You can provide excellent leadership to not only your project teams, but also to clients. You are excited and enthusiastic. You motivate your teams to do great work and collaborate easily with your clients. Most of all, you want to do it in a place where you’re more than an employee number. A place you love working.


    Still here? Good. Because if this is you, we’d really like to meet you.


    What will you be doing?


    You will be responsible for developing drug supply planning strategy and overall management of supplies for clinical studies.


    What do you need to have?

    • Assemble clinical supplies.
    • Document the assembling of clinical supplies.
    • Perform labeling operations as required.
    • Order study supplies and make them available when needed.
    • Maintain accurate and current inventory records.
    • Produce printed labels for use in labeling operations after designing labels based on approved label text and appropriate product specifications.
    • Ship study supplies in a timely manner.
    • Follow Current Good Manufacturing Practices and practice core competencies of safety and quality in performing job duties.
    • Coordinate the destruction of clinical supplies upon written instruction.
    • Attend mandatory cGMP, safety and required training.
    • Attend departmental, project and other meetings as scheduled.
    • Maintain a safe work environment for all employees in Clinical Supplies Group.
    • Interact with RD& Compliance as required.


    • HS diploma required 
    • Read, write and speak fluent English language.
    • 1-3 years applicable experience in GMP environment preferred
    • SAP experience a plus
    • 4 year degree preferered
    • Prior experience in planning, labeling, packaging, and shipping of clinical supplies and work experience in a regulated environment preferred.


    To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status.

    PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.



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