Clinical Scientist/Sr. Clinical Scientist - Oncology - Home-based anywhere in the US - FSP

Parexel; Madison (WI); Sur place; USD 90 000 - 120 000; Plein temps

Résumé du poste

Parexel in the United States seeks a Clinical Scientist to assist the Protocol Lead and study team with the clinical and scientific conduct of clinical studies, including adjudication support, medical monitoring, imaging data reconciliation, and meeting materials preparation.

The role involves collaboration with cross-functional teams and external stakeholders to ensure study objectives are met and Parexel standards are followed.

Qualifications

• Pharmaceutical experience is beneficial but not required.
• Oncology experience is required.
• 2 years medical monitoring experience preferred.
• Experience with adjudication support, medical monitoring, imaging data reconciliation and protocol deviation management.

Responsabilités

• Clinical trial 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 teams and external stakeholders.
• Supports study objectives through medical monitoring and data reconciliation.

Connaissances

Oral and written communication

MS Office (Word, Excel, PowerPoint)

Advanced Excel (Pivot Tables, VLOOKUPs

English proficiency

Willingness to travel

Formation

Life Sciences degree (BS/MS/PhD)

Bachelor's with significant clinical development experience (>5 years)

Description du poste

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.