Clinical Scientist

Clinical Scientist

Vita Global Sciences, a Kelly Company

Provided pay range:
Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

$60.09/hr - $60.09/hr

• 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.

• At least 2 years of Pharmaceutical and/or clinical drug development experience within the last 5 years (including pharmaceutical/biopharma companies, hospital settings, research sites, clinical trial units, CRO, SMO).
• 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, and identifying data errors requiring clarification with study sites – required.
• Proficient in reviewing patient data and resolving discrepancies in adverse events, adverse event trends, endpoint management, and laboratory data – preferred.
• Demonstrated oral and written communication skills.
• Proficiency in Microsoft Office (Outlook, Word, Excel and PowerPoint) required;
  One Note experience preferred.

• Degree in Life Sciences – BS/BA/MS/PhD.

This role is full‑time and offers full benefit options, including medical, dental, vision, 401(K), and paid time off (holiday, vacation, sick/personal time).

Applicants must be currently authorized to work in the US on a full‑time basis now and in the future.