Clinical Scientist- FSP

Parexel; Lincoln (NE); A distancia; USD 90.000 - 120.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Remote work

Descripción de la vacante

Parexel is seeking a Clinical Scientist to support the clinical and scientific conduct of studies, including medical monitoring, data reconciliation, and protocol deviation management.

The role involves liaising with cross-functional teams, study sites, and committees to achieve clinical objectives while adhering to Parexel processes and ICH-GCP requirements. Travel may be required as needed.

Formación

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

Responsabilidades

• Clinical trial operational delivery and study support
• Lead a study with limited scope when required
• Liaises with cross-functional teams to support study objectives
• Interacts with study sites, committees and external stakeholders
• Maintains Parexel processes and ICH-GCP compliance

Conocimientos

Oral communication

Written communication

MS Office

English proficiency

Local language

Willingness to travel

Educación

Life Sciences degree

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.