Kelly

Clinical Scientist

Kelly Philadelphia, PA

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Kelly provided pay range

This range is provided by Kelly. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$120,000.00/yr - $125,000.00/yr

Clinical Scientist


Kelly Science and Clinical FSP is currently seeking a Clinical Scientist for a long-term engagement with one of our Global Pharmaceutical clients. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc. This role is full-time and is offering full benefit options. As a Kelly FSP employee you may be eligible for Medical, Dental, Vision, 401K and a variety of other benefits to choose from. You may also be eligible for paid time off, including holiday, vacation, and sick/personal time.


(Clinical Research/Clin Ops)

Description of Services


  • Assists the CS Protocol Lead and study team with the clinical/scientific conduct of clinical studies e.g, adjudication support, medical monitoring, imaging data reconciliation preparation of meeting materials, protocol deviation management
  • May support a single study or multiple studies
  • May lead a study with limited scope (e.g., Survival Follow-up)
  • May interact with internal and external stakeholders (study sites, committees, etc.) in support of clinical study objectives


Minimum Years of Experience


  • At least 2 years Pharmaceutical and/or clinical drug development experience (such as pharmaceutical/biopharma companies, hospital settings, research sites, clinical trial units, CRO, SMO) in the last 5 years, required
  • TA-specific experience required for postings in Oncology. TA-specific experience in IDV and GSM preferred
  • Indication specific experience preferred
  • Experience reviewing and resolving study related data issues such as: issued queries, resolved queries, accurate review of medical records, identify any errors in data by performing data review that require further clarification with the study sites, etc., required
  • Proficient in reviewing patient data and resolving discrepancies in the following areas: adverse events, trends of adverse events, end point management, labs experience, preferred
  • Demonstrated oral and written communication skills
  • Proficiency in Microsoft Office (Outlook, Word, Excel and PowerPoint) required. One Note experience preferred.


Educational Requirements


  • Degree in Life Sciences
  • BS/BA/MS/PhD
  • Seniority level

    Associate
  • Employment type

    Full-time
  • Job function

    Research, Analyst, and Information Technology
  • Industries

    Staffing and Recruiting

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