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Job Requirements of Pharmacovigilance Specialist I:
-
Employment Type:
Contractor
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Location:
Clay City, IN (Onsite)
Do you meet the requirements for this job?

Pharmacovigilance Specialist I
BCforward
Clay City, IN (Onsite)
Contractor
Pharmacovigilance Specialist I BCforward is currently seeking a highly Pharmacovigilance Specialist I for an opportunity in Remote EST/CST Preferred!
Job Title: Pharmacovigilance Specialist I
Location: Remote (Nationwide, EST/CST Preferred)
Duration: 4 months
Pay Rate: $18/hour w2
Start Date: April 28, 2025
Position PurposeThe Pharmacovigilance Specialist I is responsible for monitoring and reporting adverse events or side effects of pharmaceutical products. This role involves collecting, processing, and distributing adverse event reports received from healthcare professionals and consumers. The specialist will prepare and submit reports to pharmaceutical clients or the FDA and ensure compliance with safety regulations and reporting standards. Key Responsibilities
SkillRequired Proficiency
Computer & Data EntryBasic knowledge and keyboarding skills
Microsoft Office SuiteProficient in Outlook, Word, and Excel
Attention to DetailStrong ability to identify and correct errors
Organization & PrioritizationAbility to multitask efficiently
CommunicationStrong verbal, written, and interpersonal skills Work Schedule & Environment
Job Title: Pharmacovigilance Specialist I
Location: Remote (Nationwide, EST/CST Preferred)
Duration: 4 months
Pay Rate: $18/hour w2
Start Date: April 28, 2025
Position PurposeThe Pharmacovigilance Specialist I is responsible for monitoring and reporting adverse events or side effects of pharmaceutical products. This role involves collecting, processing, and distributing adverse event reports received from healthcare professionals and consumers. The specialist will prepare and submit reports to pharmaceutical clients or the FDA and ensure compliance with safety regulations and reporting standards. Key Responsibilities
- Collect, monitor, process, and distribute adverse event reports.
- Prepare and submit adverse event cases to pharma clients or the FDA.
- Review safety and medical information for assigned pharmaceutical products.
- Ensure compliance with safety reporting requirements, including protocol safety components.
- Prepare and mail time-sensitive documentation related to adverse event cases.
- Perform data entry and document processing using ScriptMed, Microsoft Word, Excel, and PDFs.
- Maintain accuracy and attention to detail while handling sensitive medical data.
- High school diploma or equivalent (Associate's degree preferred).
- 1+ years of experience in pharmaceuticals or healthcare.
- Experience in medical assistance or project coordination is preferred.
- Basic knowledge of adverse events and pharmacovigilance is a plus.
SkillRequired Proficiency
Computer & Data EntryBasic knowledge and keyboarding skills
Microsoft Office SuiteProficient in Outlook, Word, and Excel
Attention to DetailStrong ability to identify and correct errors
Organization & PrioritizationAbility to multitask efficiently
CommunicationStrong verbal, written, and interpersonal skills Work Schedule & Environment
- Schedule: Monday - Friday, 8:00 AM - 4:30 PM (EST or CST)
- Overtime: Available but not required
- Work Type: Remote (Nationwide, preference for non-Florida candidates)
- Team Culture: Small, collaborative team environment with a strong focus on teamwork and support.
- Process an average of 33 reports per 8-hour shift.
- Maintain high accuracy in adverse event reporting and documentation.
- Effectively communicate with internal teams and external regulatory agencies.
- Number of Interviews: 1
- Selection Criteria:
- Proficiency in Microsoft Office Suite
- Strong attention to detail
- Basic computer and data entry skills
- Disqualifiers: Lack of proficiency in Microsoft Office
Interested candidates please send resume in Word format Please reference job code 236791 when responding to this ad.
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