Clinical Scientist - FSP

Parexel; Geldern; Remote; EUR 70.000 - 100.000; Vollzeit

Zusammenfassung

Parexel is seeking a Clinical Scientist to support the clinical/scientific conduct of oncology studies. The role emphasizes medical monitoring, adjudication support, and data reconciliation, with collaboration across study teams and external sites.

Preferred candidates have oncology experience and 2+ years in medical monitoring. Travel may be required, and flexibility for remote work is offered. Bachelor-level life sciences degrees accepted with relevant experience.

Qualifikationen

• Oncology experience is required.
• 2 years medical monitoring experience preferred.
• Experience with adjudication support, medical monitoring, imaging data reconciliation, meeting materials prep, and protocol deviation management.

Aufgaben

• 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.
• Interacts with internal and external stakeholders (study sites, committees) to support objectives.

Kenntnisse

Communication skills

MS Office experience

Advanced Excel

English proficiency

Willingness to travel

Ausbildung

Life sciences degree (BSc/MSc/PhD)

Alternative life sciences + >5 years clinical development

Tools

MS Word

MS Excel (Pivot tables, VLOOKUP)

MS PowerPoint

Jobbeschreibung

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.