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Clinical Research Specialist

Remote: 
Full Remote
Experience: 
Mid-level (2-5 years)
Work from: 
Connecticut (USA), Illinois (USA)

Offer summary

Qualifications:

University Degree, Minimum 2 years experience.

Key responsabilities:

  • Manage clinical research studies efficiently.
  • Prepare protocols and patient record forms.
  • Conduct clinical studies for medical/commercial purposes.
  • Oversee operational aspects of clinical trials.
  • Select sites and vendors; manage budgets.
Katalyst HealthCares & Life Sciences logo
Katalyst HealthCares & Life Sciences Pharmaceuticals SME https://www.katalysthls.com/
51 - 200 Employees
See more Katalyst HealthCares & Life Sciences offers

Job description

Responsibilities:
  • Site Management experience (site or sponsor).
  • Knowledge of/experience with CTMS/EDC/TMF.
  • Experience with Good Clinical Practice (GCP).
  • Oversees, designs, plans, and develops clinical evaluation research studies.
  • Prepares and authors protocols and patient record forms.
  • Conducts registered and nonregistered clinical studies of products that have been determined to satisfy a medical need and/or offer a commercial potential. Oversees and interpret results of clinical investigations in preparation for new drug device or consumer application.
  • Oversees and resolves operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific country regulations and may prepare clinical trial budgets.
  • May be responsible for clinical supply operations, site and vendor selection.
Requirements:
  • Requires a University Degree and minimum of 2 years of relevant experience.

Required profile

Experience

Level of experience: Mid-level (2-5 years)
Industry :
Pharmaceuticals
Spoken language(s):
English
Check out the description to know which languages are mandatory.

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