Clinical Research Associate - Medical Affairs - Oncology - New York / Northeast

PRA Health Sciences in Vernon Rockville, CT

  • Industry: Scientific Research - Health/Medicine/Pharmacology
  • Type: Full Time
  • Compensation: $69,840.00 - 100,940.00 / Year*
position filled

Overview



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 are 16,000+ 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.

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

Responsibilities



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.

Qualifications



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 30% or more)
  • 3+ years of clinical monitoring experience required Knowledge of ICH and local regulatory authority regulations regarding drug PREFERRED
  • ONCOLOGY EXPERIENCE HIGHLY PREFERRED including 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.

PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.
Associated topics: clinical, dietician, disease, drug discovery, histology, histotechnologist, microbiological, nephrology, pharmacy, vaccine

* Estimated salary


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