Clinical Scientist- FSP

Parexel; Brewster Heights (NY); Remote; USD 90.000 - 120.000; Vollzeit

Zusammenfassung

Parexel is seeking a Clinical Scientist to support protocol conduct, medical monitoring and data reconciliation across clinical studies. You will assist the Protocol Lead, prepare materials for meetings and help manage deviations while liaising with study teams and external sites.

You should have a life sciences degree and 2+ years of experience; pharma exposure is beneficial. Strong communication and MS Office skills are required, and willingness to travel for key company meetings.

Qualifikationen

• Strong written and oral communication skills.
• MS Office Proficiency (Word, Excel, PowerPoint).
• Fluent in English; local language where applicable.

Aufgaben

• Clinical Trial Operational Delivery: support single or multiple studies and liaise with cross-functional teams.
• May lead a study with limited scope (e.g., Survival Follow-up).
• Interact with internal/external stakeholders (sites, committees) to meet study objectives.
• Ensure compliance with Parexel processes and ICH-GCP guidelines.

Kenntnisse

Communication skills

MS Office Suite

English proficiency

Willingness to travel

Local language familiarity

Ausbildung

Life Sciences degree (BSc/MSc/PhD)

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

Jobbeschreibung

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.