Safety Surveillance Support Specialist
About this role
Description
Safety Surveillance Support Specialist
Venesco LLC is seeking a Safety Surveillance Support Specialist to support pharmacovigilance and clinical safety activities by processing safety reports, monitoring adverse event information, maintaining safety databases, and supporting regulatory reporting requirements.
Requirements
Duties and Responsibilities
- Monitor safety email inboxes and reporting systems.
- Receive and triage adverse event reports.
- Process safety cases and follow-up information.
- Support MedWatch and regulatory reporting submissions.
- Reconcile clinical and safety databases.
- Maintain safety documentation and records.
- Support DSMB preparation and logistics.
- Assist with safety trend analysis.
- Support annual safety reports and study closeout activities.
- Ensure documentation is inspection ready.
Minimum Qualifications
- Bachelor's degree in Life Sciences, Nursing, Public Health, or related field.
- Minimum 3 years of pharmacovigilance or drug safety experience.
- Familiarity with Argus or similar safety systems.
- Knowledge of FDA and ICH safety reporting requirements.
Venesco, LLC, is an equal opportunity and affirmative action employer. Venesco is committed to administering all employment and personnel actions on the basis of merit and free of discrimination based on race, ethnicity, religious affiliation, gender, gender identity or expression, sexual orientation, national origin, protected veteran status, or status as an individual with a disability. Consistent with this commitment, we are dedicated to the employment and advancement of qualified minorities, women, individuals with disabilities, protected veterans, persons of all ethnic backgrounds and religions according to their abilities.
For more information on Venesco, LLC., visit https://venesco.com.
Company at a glance
Venesco, LLC is a premier government contractor delivering Healthcare, IT, Research & Development, and a range of mission‑critical services to federal agencies. For more than 18 years, we’ve evolved from a small consulting firm into a respected leader in biomedical R&D and IT support, backed by strong financials, mature processes, and a commitment to employee connectedness and work–life balance.
Our success is driven by our skilled professionals, agile management practices, and high‑quality standards. Venesco holds a Top‑Secret Facility Clearance and maintains CMMI® Maturity Level 3 (Services) and ISO 9001:2015 and 14001:2015 certifications. We’ve been recognized on the Inc. 5000 and Washington Technology’s Fast 50 lists for five consecutive years.
With more than 350 credentialed employees and 65+ prime contracts — ranging from small teams to programs with 150+ personnel — we deliver the impact of a large enterprise while maintaining the agility of a small business. Venesco continues to recruit motivated, talented individuals who want to contribute to meaningful federal initiatives and join a collaborative, high‑performing team.
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