Clinical Scientist- FSP

Parexel; Dover (DE); Teletrabalho; USD 90 000 - 130 000; Tempo integral

Resumo da oferta

Parexel is seeking a Clinical Scientist to support clinical studies under the guidance of the Protocol Lead. The role involves medical monitoring, adjudication support, and preparation of materials for study oversight. Strong communication in English and MS Office proficiency are essential.

Travel is anticipated to support key company meetings and cross-site collaboration. Applicants with life sciences degrees and relevant clinical development experience are preferred.

Qualificações

• 2+ years medical monitoring experience preferred.
• TA-specific experience beneficial.
• Pharmaceutical experience beneficial but not required.

Responsabilidades

• Assist the Protocol Lead and study team with the clinical/scientific conduct of clinical studies.
• Provide adjudication support, medical monitoring and data reconciliation.
• Prepare meeting materials and manage protocol deviations.
• Liaise with cross-functional teams and stakeholders to support study objectives.
• Maintain compliance with Parexel standards, ICH-GCP and applicable requirements.
• Interact with study sites, committees and other external partners as needed.

Conhecimentos

Oral and written communication

English proficiency

Willingness to travel

Formação académica

Bachelor/Master/PhD in Life Sciences

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

Ferramentas

MS Office Suite (Word, Excel, PowerPoint)

Descrição da oferta de emprego

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.