Clinical Research Associate – Early Development Oncology

  • 3 years ago

Job Information

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    No. of Openings 1 opening
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    Job Experience 2 years
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    Education Level Some college
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    Location Restrictions USA only

Job Description

Calling ALL Experienced Clinical Research Associates – Read On, Join the Movement

We believe that our people are the future of the industry. We provide a culture in which our employees can enjoy personal satisfaction, professional achievement and have the ability to strategically map out long-term career plans. If you’re ready to be a part of something inspiring join us and Discover Your PRA.

Who are we?

We Are PRA.

We are16,000+ employees strong, operating in more than90+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.

What’s in it for you in the long term?

  • We promote from within – We provide a career, not a job.
  • Culture – There is nothing like it. We have many former PRA employees returning every single month.
  • Tools and Technology – Leading the industry with time-saving, intuitive smart technology to help predict trends, anticipate needs and eliminate the need for multiple data entry.
  • Security – We are growing and we are dedicated to having you grow with us.
  • Mentorship and Training – Our structure provides support for your growth and development as well as questions that arise while on a study at all times.
  • Work/Life Balance – It’s real; we value it. Our strategic solutions and full-service models offer you choices for finding a career that includes time for your personal life.
  • Salary/ Benefits- We are committed to providing our employees with a competitive salary and benefits package with yearly merit and performance reviews.


Education: Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (i.e., registered nurse); or equivalent work experience

Required Skills:

  • Read, write and speak fluent English; fluent in host country language required.
    2+ years of clinical monitoring experience required
  • Knowledge of ICH and local regulatory authority regulations regarding drug
  • Clinical research experience
  • Knowledge of ICH and local regulatory authority regulations regarding drug
  • Experience in monitoring all trial components (PSSV to COV)
  • Ability to travel as needed (greater than 50%)
  • 3+ years of clinical monitoring experience required Knowledge of ICH and local regulatory authority regulations regarding drug PREFERRED
  • Phase I experience highly preferred; Immunology experience is ideal as well.
  • All therapeutic experience is welcome – ONCOLOGY EXPERIENCE PREFERREDincluding but not limited to: Oncology, Hematology, Respiratory, Cardiovascular, Pain, CNS, Infectious Disease, Metabolism, Vaccines, Transplant and Ophthalmology

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.

The Clinical Research Associate (CRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements. This role will focus on Early Development Oncology studies.

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