Clinical Scientist- FSP

Parexel; Pierre (SD); Remote; USD 85,000 - 115,000; Full time

Job summary

Parexel is hiring a Clinical Scientist to assist the Protocol Lead and study team in the clinical/scientific conduct of studies, including medical monitoring, adjudication support, and data reconciliation.

The role involves supporting a study or multiple studies, liaising with cross-functional lines, and traveling to key meetings as required. Strong communication and MS Office skills are essential, with a life sciences background or significant clinical development experience preferred.

Qualifications

• 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 for key meetings.

Responsibilities

• Support clinical trial operational delivery for one or more studies.
• Assist in medical monitoring, adjudication support, and data reconciliation.
• Liaise with cross-functional teams and external stakeholders to meet study objectives.
• Adhere to Parexel processes and ICH-GCP requirements.

Skills

Communication

MS Office

English proficiency

Local language

Travel readiness

Education

Life Sciences degree (Bachelors/Masters/PhD)

Alternative: >5 years clinical development experience

Job description

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.