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Clinical Scientist - FSP

Parexel

Montpelier, VTJobSeen 3 days agoSeen in employer's feed 1 day ago

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At a glance

Compensation
No compensation found
Location
Montpelier, VT
Work Authorization
Not specified

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Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

The Clinical Scientist supports the protocol lead and study team in the scientific conduct of oncology clinical studies, providing adjudication support, medical monitoring, imaging data reconciliation, and protocol deviation management while ensuring compliance with Parexel standards and processes.

Skills & qualifications

RequiredNice to have

Skills

Oral and Written CommunicationMs Office SuiteAdvanced ExcelEnglish ProficiencyWillingness to Travel

Qualifications

Oncology ExperienceTwo Years Medical Monitoring ExperiencePharmaceutical ExperienceBachelors Masters Phd in Life SciencesBachelor's Degree With Significant Clinical Development Experience

Full job description

Oncology experience preferred

Job Purpose:

The Clinical Scientist (CS) 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).

Key Accountabilities:

May include but not limited to the following:

Clinical Trial Operational Delivery

  • 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

Compliance with Parexel Standards

  • 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,

ICH-GCPs and other applicable requirements

Skills:

  • 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

  • Willingness to travel as required for key company meetings

Knowledge and Experience:

  • Pharmaceutical experience beneficial but not required

  • Oncology experience is required

  • 2 years medical monitoring experience preferred

  • Experience with adjudication support, medical monitoring, imaging data reconciliation preparation of meeting materials, and protocol deviation management

Education:

  • 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)

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EEO Disclaimer

Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

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