Alpha Consulting Corp. · 1 month ago
Assoc Clinical Research Specialist
Minneapolis, MN
Full-time
Onsite
New Grad, Entry, Mid Level
0+ years expAlpha Consulting Corp. is seeking an Associate Clinical Research Specialist to support the management of clinical study safety data. This role involves partnering with cross-functional teams to manage adverse event reporting and ensure compliance with regulatory requirements throughout the clinical study lifecycle.
ConsultingPharmaceuticalStaffing Agency
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
Alpha Consulting Corp.
Alpha Consulting Corp. has been exceeding expectations in the IT, pharmaceutical, and clinical staffing business since 1994.
201-500 employees
H1B Sponsorship
Alpha Consulting Corp. has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (2)
2024 (4)
2023 (3)
2021 (4)
2020 (6)
Funding
Current Stage
Growth StageCompany data provided by crunchbase