Clinical Scientist- FSP

Parexel; Boston (MA); Remote; USD 90,000 - 130,000; Full time

Job summary

Parexel is hiring a Clinical Scientist to support the clinical/scientific conduct of studies, including adjudication and medical monitoring. The CS will work with the protocol lead and study team, liaising with cross-functional partners and external sites to meet study objectives.

Requirements include a Life Sciences degree with 2+ years of experience or substantial clinical development experience, strong communication skills, and willingness to travel as needed. Remote-work option available.

Qualifications

• Bachelor's/Master's/PhD in Life Sciences with 2+ years relevant experience.
• If no Life Sciences degree, >5 years of clinical development experience.
• 2 years medical monitoring experience preferred.

Responsibilities

• Assist the CS Protocol Lead and study team with the clinical/scientific conduct of clinical studies, including adjudication support, medical monitoring, and data reconciliation.
• Support a single study or multiple studies; may lead a study with limited scope.
• Liaise with cross-functional teams and interact with study sites and committees to achieve study objectives.
• Maintain Parexel processes and ensure compliance with ICH-GCPs and applicable requirements.

Skills

Oral and written communication

MS Office

English proficiency

Local language

Travel willingness

Education

Life Sciences degree

Clinical development experience (>5 years) if no Life Sciences degree

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.