Clinical Supply Specialist - Label and Translation Coordinator at Pharmaceutical Research Associates, Inc. in HORSHAM, Pennsylvania

Posted in Supply Chain 18 days ago.





Job Description:

Pharmaceutical Research Associates, Inc.

Clinical Supply Specialist - Label and Translation Coordinator

US-PA

Job ID: 2020-68749
Type: US-Southeast
# of Openings: 1
Category: Logistics

Merck

Overview

Who are we?

We Are PRA.

We are 18,000+ employees strong, operating in more than 90+ 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 help get life-saving drugs into the hands of 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.



Responsibilities

Works in partnership with the scientific, business, operational, clinical and technology areas to support the execution of global clinical trials in the area of global clinical supply management. This includes management of the planning/forecasting, packaging/labeling, distribution and return of clinical supplies for phase 1-IV clinical trials.

Demonstrated ability to navigate clinical inventory management and IVRS systems

Proficient in computer skills including Microsoft applications
Demonstrated knowledge of clinical supply chain logistics process
Demonstrated understanding of local country regulations
Strong technological skills and ability to learn and adapt quickly.
Effective clinical supply management skills.
Demonstrated organizational skills and ability to multi-task
Proficient in following Standard Operating Procedures (SOP's)
Demonstrated ability to communicate clearly, effectively and tactfully.
Demonstrated ability to interact with different professional levels of the medical community
Demonstrated ability to think logically and to critically evaluate and solve problems



Qualifications

  • Bachelor’s Degree from an accredited institution required
  • Basic knowledge of clinical drug trials preferred
  • Good understanding of medical terminology preferred
  • Effectively demonstrates oral and written communication skills
  • Applies proficient time management knowledge of database and spreadsheet systems. e.g. Word, Excel, Access and Outlook
  • Efficient in creating recruiting documents
  • 2 years of equivalent work experience 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.

PI124697492