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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. This role is based out of the PA/NY/NJ region - US.

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%)
  • 3+ yearsof clinical monitoring experience required Knowledge of ICH and local regulatory authority regulations regarding drugPREFERRED
  • 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.


    Associated topics: aoa, breast, cancer, hem onc, hematology, lah, oncology, palliative, physician md, thedacare

    * The salary listed in the header is an estimate based on salary data for similar jobs in the same area. Salary or compensation data found in the job description is accurate.

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