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Entry-Level Clinical Research

There is a high demand for trained professionals in Entry-Level Clinical Research jobs. A Bachelor of Science degree is a must to apply for this position. Ideally, the industry is looking for science graduates from Pharmacy, Medicine, Life Science, and Bioscience. Individuals applying for the Entry-Level Clinical Research position should have two to three years? prior work experience. The most common Entry-Level Clinical research position is that of a Clinical Research Associate (CRA), who specializes in designing, implementing, planning, and monitoring clinical trials. The CRA ensures that good clinical practices are followed. Biostatistician is another position in the Entry-Level Clinical Research field. A Biostatistician is responsible for performing statistical programming, design, and analysis for clinical trial projects. In addition, the Biostatistician is responsible for submitting new drug applications and biological license applications. Another Entry-Level Clinical Research position is that of Clinical Research Manager (CRM). Candidates for this position should be able to supervise others in designing and writing protocols, case report forms, and informed consent forms for clinical trials. The CRM ensures that Case Report Forms are reviewed in a timely fashion and submitted to the data management group. If your qualifications include a Master\'s degree, then the amount of remuneration almost doubles in each Entry-Level Clinical Research position. Clinical research is an industry where experience counts; thus the longer you are in this field, the higher the salary you can expect.

Search related to:

Contract Clinical Research
Home-Based Clinical Research

Related Jobs 1 matches

  • Clinical Trials Specialist - Entry Level Opportunity, Rockville, MD
    Rockville, MD
    E5041:Regulatory Doc Analyst Asc Job Description Opportunity supporting the NCI's Clinical Trials Reporting Program (CTRP) by reviewing clinical protocols and other regulatory documents that impact the registration of clinical trials into CTRP. Responsible for interpreting clinical and scientific data for trial abstracts, including but not limited to, writing, editing, and..




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