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PAREXEL

Clinical Scientist - FSP

nashville, TN

Check who can apply and the requirements below before continuing.

About this opportunity

PAREXEL lists this Clinical Scientist - FSP opportunity in nashville, Tennessee. Review the employer’s description below for duties, qualifications and application requirements.

Job description

Job Overview:

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:

Clinical Trial Operational Delivery

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

May support a single study or multiple studies

May lead a study with limited scope (e.g., Survival Follow-up)

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 and timely 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:

Proficient in reviewing patient data and resolving discrepancies in the following areas such as adverse events, trends of adverse events, end point management, labs experience preferred 

Demonstrated oral and written communication skills 

Proficiency in Microsoft Office (Outlook, Word, Excel and PowerPoint) required. One Note experience preferred. 

Knowledge and Experience:

At least 2 years Pharmaceutical and/or clinical drug development experience (such as pharmaceutical/biopharma companies, hospital settings, research sites, clinical trial units, CRO, SMO) in the last 5 years required 

TA-specific experience required for postings in Oncology IDV and GSM preferred. 

Indication specific experience preferred 

Experience reviewing and resolving study related data issues such as issued queries, resolved queries, accurate review of medical records, identify any errors in data by performing data review that require further clarification with the study sites, etc. required 

Education:

Degree in Life Sciences 

Bachelor of Science/Bachelor of Arts/Master of Science/PhD 

#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.

Worksite address

nashville, TN, 37247, US

Who can apply

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