FREE ACCESS
5,000–10,000 jobs/day
See all jobs on Scoutfield
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical study support, including medical monitoring, adjudication activities, and protocol deviation management. Proficient in ICH-GCP compliance and skilled in preparing meeting materials and imaging data reconciliation.
Highest-signal resume keywords
Oncology ExperienceMedical Monitoring ExperienceAdjudication SupportAdvanced Excel SkillsLife Sciences Degree
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Study SupportProtocol Deviation ManagementImaging Data ReconciliationMedical MonitoringAdjudication Activities
Soft Skills
Oral Communication SkillsWritten Communication Skills
Tools & Technologies
MS Office SuiteExcel Pivot TablesVLOOKUP
Industry Keywords
ICH-GCP ComplianceClinical DevelopmentPharmaceutical ExperienceParexel ProcessesLife Sciences
About the role
Key responsibilities & impact- Assist the CS Protocol Lead and study team with the clinical/scientific conduct of clinical studies
- Support adjudication activities
- Support medical monitoring
- Prepare for imaging data reconciliation
- Prepare meeting materials
- Manage protocol deviations
- Support a single study or multiple studies
- Lead studies with limited scope, such as Survival Follow-up
- Liaise with cross-functional lines
- Interact with internal and external stakeholders, including study sites and committees, in support of clinical study objectives
- Complete required training, timesheets, and expense reports
- Update CV as required
- Comply with Parexel processes, ICH-GCPs, and other applicable requirements
Requirements
What you’ll need- Oncology experience is required
- 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)
- Demonstrated oral and written communication skills
- MS Office Suite experience, including Word, Excel, and PowerPoint
- Advanced Excel skills, including pivot tables and VLOOKUPs
- Proficient in written and spoken English
- Willingness to travel as required for key company meetings
- Pharmaceutical experience beneficial but not required
- 2 years medical monitoring experience preferred
- Experience with adjudication support, medical monitoring, imaging data reconciliation, preparation of meeting materials, and protocol deviation management
- Maintains working knowledge of and complies with Parexel processes, ICH-GCPs, and other applicable requirements
Benefits
Comp & perks- Equal opportunity employment
- Home-based/remote work arrangement
