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Survival Follow-upPosted 23 days ago

Clinical Scientist - FSP

Full-time
Remote
2+ years
Competitive
Posted 23 days ago

Parexel is seeking a Clinical Scientist to support the clinical and scientific conduct of oncology clinical studies. The role assists the Clinical Scientist Protocol Lead and study team with operational delivery, adjudication support, medical monitoring, imaging data reconciliation, meeting materials, and protocol deviation management.

Posted
23 days ago
Source
jobs.parexel.com
Sector
Healthcare

Opens the employer's application page in a new tab

Responsibilities

  • May support a single study or multiple studies
  • May lead a study with limited scope (e.g., Survival Follow-up)
  • Liaises with cross-functional lines as appropriate
  • May interact with internal and external stakeholders (study sites, committees, etc.) in support of clinical study objectives
  • Complies with required training curriculum
  • Completes timesheets accurately as required
  • Submits expense reports as required
  • Updates CV as required
  • Maintains a working knowledge of and complies with Parexel processes

Qualifications

  • Demonstrated oral and written communication skills
  • MS Office Suite Experience Required– including Word, Excel, and Power Point
  • Advanced Excel skills required (pivot tables, v-lookups)
  • Proficient in written and spoken English
  • Oncology experience is required
  • Experience with adjudication support, medical monitoring, imaging data reconciliation preparation of meeting materials, and protocol deviation management
  • Bachelors/Masters/PhD in Life Sciences with 2+ years relevant career experience
  • If no degree in Life Sciences, must have Bachelor's degree with significant experience in clinical development (>5 years)

Preferred

  • Oncology Experience Preferred
  • Pharmaceutical experience beneficial but not required
  • 2 years medical monitoring experience preferred
  • Pharmaceutical Experience
  • Medical Monitoring Experience

Required skills

Adjudication SupportAdvanced ExcelClinical Trial OperationsImaging Data ReconciliationMedical MonitoringMicrosoft ExcelMicrosoft PowerPointMicrosoft WordOncologyProtocol Deviation Management

Nice to have

(31)(38)(41)(46)*20262023202420253.871Accounting and FinanceCustomer Service and SupportData Powered byEducation and Training

Full job description

Parexel is seeking a Clinical Scientist to support the clinical and scientific conduct of oncology clinical studies. The role assists the Clinical Scientist Protocol Lead and study team with operational delivery, adjudication support, medical monitoring, imaging data reconciliation, meeting materials, and protocol deviation management.

Responsibilities

  • May support a single study or multiple studies
  • May lead a study with limited scope (e.g., Survival Follow-up)
  • Liaises with cross-functional lines as appropriate
  • May interact with internal and external stakeholders (study sites, committees, etc.) in support of clinical study objectives
  • Complies with required training curriculum
  • Completes timesheets accurately as required
  • Submits expense reports as required
  • Updates CV as required
  • Maintains a working knowledge of and complies with Parexel processes

Preferred

  • Oncology Experience Preferred
  • Pharmaceutical experience beneficial but not required
  • 2 years medical monitoring experience preferred
  • Pharmaceutical Experience
  • Medical Monitoring Experience

Company

  • Global clinical research and biopharmaceutical services company
  • Raleigh, North Carolina, USA
  • http://www.parexel.com/
  • Founded in 1983
  • 10001+ employees

Qualifications

  • Demonstrated oral and written communication skills
  • MS Office Suite Experience Required– including Word, Excel, and Power Point
  • Advanced Excel skills required (pivot tables, v-lookups)
  • Proficient in written and spoken English
  • Oncology experience is required
  • Experience with adjudication support, medical monitoring, imaging data reconciliation preparation of meeting materials, and protocol deviation management
  • Bachelors/Masters/PhD in Life Sciences with 2+ years relevant career experience
  • If no degree in Life Sciences, must have Bachelor's degree with significant experience in clinical development (>5 years)
  • Oncology Experience Preferred
  • Pharmaceutical experience beneficial but not required
  • 2 years medical monitoring experience preferred

Required skills

  • Adjudication Support, Advanced Excel, Clinical Trial Operations, Imaging Data Reconciliation, Medical Monitoring, Microsoft Excel, Microsoft PowerPoint, Microsoft Word, Oncology, Protocol Deviation Management

Preferred skills

  • (31), (38), (41), (46), *2026, 2 years medical monitoring experience preferred, 2023, 2024, 2025, 3.8, 71, Accounting and Finance, Customer Service and Support, Data Powered by, Distribution of Different Job Fields Receiving Sponsorship, Education and Training, Engineering and Development, Glassdoor, H1B Sponsorship, Human Resources, Legal and Compliance, Management and Executive, Marketing, Oncology Experience Preferred, Pharmaceutical experience beneficial but not required, Raleigh, North Carolina, USA, Represents job field similar to this job, Sales, Trends of Total Sponsorships, http://www.parexel.com

Experience

  • 2+ years

Job details

Employment type

Full-time

Seniority level

2+ years

Date posted

Oct 21, 2026

Work mode

Remote

Job source

jobs.parexel.com

Company

Survival Follow-up

Healthcare

Global clinical research and biopharmaceutical services company

  • Raleigh, North Carolina, USA
  • Healthcare
  • 10001+ employees
  • Founded 1983
  • parexel.com

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