Clinical Scientist- FSP

Parexel; Phoenix (AZ); Teletrabalho; USD 85 000 - 120 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Remote work

Travel opportunities

Competitive benefits

Resumo da oferta

Parexel is seeking a Clinical Scientist in the United States for clinical trial oversight and scientific support. You will assist the Protocol Lead and study team with medical monitoring, adjudication support, and data reconciliation across studies.

Requirements include a Life Sciences degree with 2+ years of relevant experience, strong English communication, and proficiency in MS Office. Some travel may be required to support key company meetings.

Qualificações

• Bachelor's/Master's/PhD in Life Sciences with 2+ years of relevant experience.
• Pharmaceutical/clinical development experience beneficial but not required.
• Strong written and verbal communication skills.

Responsabilidades

• Support clinical trial operational delivery across one or more studies.
• Assist with medical monitoring, data reconciliation, and meeting material prep.
• Coordinate with internal/external stakeholders and travel as needed.
• Ensure Parexel processes and ICH-GCP compliance are followed.

Conhecimentos

Oral and written communication

English proficiency

Willingness to travel

Formação académica

Life Sciences degree

Ferramentas

MS Office

Descrição da oferta de emprego

PXL is hiring a Clinical Scientist!

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
• Proficient in written and spoken English
• Proficient in local language (as applicable)
• Willingness to travel as required for key company meetings

Knowledge and Experience:

• Pharmaceutical experience beneficial but not required
• Therapeutic Area (TA) specific experience beneficial
• 2 years medical monitoring experience preferred

Education:

• Bachelors/Masters/PhD in Life Sciences with 2+ years relevant career experience
• If no degree in Life Sciences, must have significant experience in clinical development (>5 years)

#LI-REMOTE

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.