Scalence L.L.C. · 1 month ago
Assoc Clinical Research Specialist
Minneapolis, MN
Full-time
Onsite
New Grad, Entry, Mid Level
0+ years expScalence L.L.C. is seeking an Associate Clinical Research Specialist to support the management of clinical study safety data. This role involves collaborating with cross-functional teams to manage adverse event reporting and ensure compliance with regulatory requirements.
Information Technology & Services
Responsibilities
Review and assess Adverse Events (AEs), Serious Adverse Events (SAEs), and device deficiencies
Identify potential complaints and unreported safety events from CRFs
Collaborate with Regulatory Affairs and complaint teams for timely safety reporting
Communicate with clinical sites and monitors for follow-up information
Support safety documentation, reports, and audits
Qualification
Required
Science, nursing, or medical background
Experience with clinical databases (e.g., RAVE, Veeva Vault)
Strong written and verbal communication skills
Ability to review and assess clinical safety data (AEs/SAEs)
Knowledge of clinical research regulations and compliance
Bachelor's degree required
0–5 years of clinical research or safety experience
Company
Scalence L.L.C.
In today’s dynamic and competitive market, success hinges on mastering three key areas: Data Intelligence, Business Resilience, and Digital Experience.
501-1000 employees
Funding
Current Stage
Late StageCompany data provided by crunchbase