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Clinical Scientist

  • Clinical Scientist job type Posted on: Nov 03, 2026
  • Clinical Scientist experience level Kelly Science, Engineering, Technology & Telecom
  • Clinical Scientist employment type United States, Pennsylvania
  • Clinical Scientist employment type Onsite
  • Clinical Scientist salary Full-time

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Job Title :

Clinical Scientist

Job Type :

Full-Time

Job Location :

United States Pennsylvania United States

Remote :

No

Jobcon Logo Job Description :

Clinical ScientistKelly Science & Clinical FSP is seeking a Clinical Scientist for a long-term remote engagement supporting a global pharmaceutical client. This individual will work closely with the Clinical Scientist Protocol Lead and study team to support the clinical and scientific execution of clinical studies.Key ResponsibilitiesAssist the Clinical Scientist Protocol Lead and study team with the clinical/scientific conduct of clinical studiesSupport medical monitoring activities, adjudication, imaging data reconciliation, and preparation of study meeting materialsReview clinical study data and assist with identification and resolution of data discrepancies and queriesSupport protocol deviation review and managementReview patient data, including adverse events, laboratory results, endpoints, and other clinical informationSupport one or multiple clinical studies depending on study needsMay lead a study or workstream with limited scope, such as survival follow-upInteract with internal and external stakeholders, including study sites and committees, to support clinical study objectivesQualificationsDegree in Life Sciences required (BS/BA/MS/PhD)Minimum of 2 years of pharmaceutical and/or clinical drug development experience within the last 5 yearsExperience may come from pharmaceutical/biopharmaceutical companies, CROs, hospitals, research sites, clinical trial units, or SMOsExperience reviewing and resolving study-related data issues, including queries and medical record/data reviewAbility to identify data discrepancies requiring clarification with clinical study sitesExperience reviewing patient data and resolving discrepancies involving adverse events, laboratory results, endpoints, and safety data preferredTherapeutic-area experience required for Oncology positions; indication-specific experience preferredStrong written and verbal communication skillsProficiency with Microsoft Outlook, Word, Excel, and PowerPoint; OneNote experience preferred

Jobcon Logo Position Details

Posted:

Nov 03, 2026

Reference Number:

10440_4459419292

Employment:

Full-time

City:

United States

Job Origin:

APPCAST_CPC

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Clinical ScientistKelly Science & Clinical FSP is seeking a Clinical Scientist for a long-term remote engagement supporting a global pharmaceutical client. This individual will work closely with the Clinical Scientist Protocol Lead and study team to support the clinical and scientific execution of clinical studies.Key ResponsibilitiesAssist the Clinical Scientist Protocol Lead and study team with the clinical/scientific conduct of clinical studiesSupport medical monitoring activities, adjudication, imaging data reconciliation, and preparation of study meeting materialsReview clinical study data and assist with identification and resolution of data discrepancies and queriesSupport protocol deviation review and managementReview patient data, including adverse events, laboratory results, endpoints, and other clinical informationSupport one or multiple clinical studies depending on study needsMay lead a study or workstream with limited scope, such as survival follow-upInteract with internal and external stakeholders, including study sites and committees, to support clinical study objectivesQualificationsDegree in Life Sciences required (BS/BA/MS/PhD)Minimum of 2 years of pharmaceutical and/or clinical drug development experience within the last 5 yearsExperience may come from pharmaceutical/biopharmaceutical companies, CROs, hospitals, research sites, clinical trial units, or SMOsExperience reviewing and resolving study-related data issues, including queries and medical record/data reviewAbility to identify data discrepancies requiring clarification with clinical study sitesExperience reviewing patient data and resolving discrepancies involving adverse events, laboratory results, endpoints, and safety data preferredTherapeutic-area experience required for Oncology positions; indication-specific experience preferredStrong written and verbal communication skillsProficiency with Microsoft Outlook, Word, Excel, and PowerPoint; OneNote experience preferred

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