Clinical Scientist - FSP

Parexel; Juneau (AK); A distancia; USD 85.000 - 105.000; Jornada completa

Descripción de la vacante

Parexel is seeking a Clinical Scientist to support the clinical/scientific conduct of studies, including medical monitoring and data reconciliation. The CS assists the Protocol Lead and study team, prepares materials for meetings, and manages protocol deviations as needed.

The role involves collaboration with internal and external stakeholders, regulatory compliance, and strong documentation. A life sciences degree with relevant experience is preferred, with remote work options available where

Formación

• Demonstrated oral and written communication skills.
• MS Office Suite Experience– Word, Excel, PowerPoint.
• Proficient in written and spoken English.
• Proficient in local language (as applicable).
• Willingness to travel as required for key company meetings.

Responsabilidades

• Support clinical trial operational delivery for one or multiple studies.
• Assist with medical monitoring and protocol adherence activities.
• Liaise with cross-functional teams and study sites to meet objectives.
• Ensure Parexel standards and training requirements are followed.

Conocimientos

Communication

MS Office

English proficiency

Travel willingness

Local language

Educación

Life Sciences degree

Clinical development experience (5+ years)

Descripción del empleo

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.