
Clinical Scientist - FSP
Dover, DEJobSeen 3 days agoSeen in employer's feed 1 day ago
Most applications go out cold — see where you stand first. No sign-up to start.
Watch jobs like this. New roles like this one near Dover, DE, by email.
Don't just apply. Show up ready.
Olive works from this exact posting.
At a glance
Olive lists jobs from US employers, including remote roles you can work from the United States.
Requirements
Credentials this posting asks for.
Job overview
The Clinical Scientist assists the protocol lead and study team with clinical and scientific conduct of oncology studies, including adjudication support, medical monitoring, imaging data reconciliation, and protocol deviation management, while ensuring compliance with Parexel standards and processes.
Skills & qualifications
Skills
Qualifications
Full job description
Oncology experience preferred
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
-
Advanced Excel skills required (pivot tables, v-lookups)
-
Proficient in written and spoken English
-
Willingness to travel as required for key company meetings
Knowledge and Experience:
-
Pharmaceutical experience beneficial but not required
-
Oncology experience is required
-
2 years medical monitoring experience preferred
-
Experience with adjudication support, medical monitoring, imaging data reconciliation preparation of meeting materials, and protocol deviation management
Education:
-
Bachelors/Masters/PhD in Life Sciences with 2+ years relevant career experience
-
If no degree in Life Sciences, must have Bachelor's degree with significant experience in clinical development (>5 years)
#LI-LG4
#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.
Similar jobs, posted recently
Open roles like this one, listed in the last 30 days.
Clinical Consultant, Medical Imaging TechnologyFujifilm · Remote · US · $93–108K/yrPosted 2w agoPosted 2w ago
Clinical Product Coordination - Associate (Location: CHICAGO)Fujifilm · Remote · US · $60–80K/yrPosted 3 days agoPosted 3 days ago
Clinical Consultant, MSFujifilm · Remote · USPosted 3w agoPosted 3w ago
Clinical Specialist (Sonographer) - Washington, DCFujifilm · Dover, DE · $90–125K/yrPosted 4 days agoPosted 4 days ago
Clinical Specialist (Sonographer) - New JerseyFujifilm · Dover, DE · $90–125K/yrPosted 4 days agoPosted 4 days ago
You've read the whole posting — now see how you match it.