Clinical Scientist - FSP

Parexel; Oregon; Híbrido; USD 90.000 - 130.000; Jornada completa

Descripción de la vacante

Parexel is seeking a Clinical Scientist to support the clinical and scientific conduct of studies, including adjudication, medical monitoring, and material preparation. You will liaise with cross-functional teams and external sites while maintaining Parexel standards.

Oncology experience is required and 2 years of medical monitoring is preferred. Travel to key meetings may be needed; a life sciences background is essential.

Formación

• Bachelor’s/Master’s/PhD in Life Sciences with 2+ years relevant experience, or a Bachelor’s with >5 years clinical development.
• Life sciences training plus clinical development knowledge desirable.

Responsabilidades

• Assist protocol lead and study team with clinical/scientific conduct.
• Provide adjudication support, medical monitoring, and meeting materials prep.
• Ensure compliance with Parexel standards and required trainings.

Conocimientos

Communication skills

MS Office

Advanced Excel

English fluency

Willing to travel

Educación

Life sciences degree

Descripción del empleo

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

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 objectivesCompliance 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)

#LI-CF1EEO DisclaimerParexel 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.