Remote Postal Data Entry Jobs in Remote, OR (NOW HIRING)

Client: Pharmaceutical Company

Type: Contract Position

Location: 100% remote, client is in NJ

The person will support adverse event intake and triage for marketed and investigational products. They will do preliminary evaluation of adverse event reports from clinical trials, post-marketing/spontaneous reports, and solicited sources.

Key duties include:

• Reviewing adverse event reports for completeness and accuracy
• Communicating with partners or affiliates when clarification is needed
• Performing duplicate searches
• Entering initial case data
• Assigning cases to Product Safety Specialists
• Helping determine seriousness, expectedness, and case validity
• Prioritizing work to meet company and regulatory deadlines
• Distributing safety information internally or externally when needed

Required Qualifications

• Bachelor’s degree required
• Scientific or medical discipline preferred
• Medical terminology knowledge
• Data coding and database retrieval experience
• Strong attention to detail
• Ability to multitask
• Good written and verbal communication skills
• Ability to work independently and as part of a team

Preferred Qualifications

• Prior Product Safety or Pharmacovigilance experience
• Experience with adverse event case processing, intake, triage, or coding

Important Recruiter Note

The ideal candidate is more likely a PV/Product Safety coordinator, case intake associate, safety data/coding specialist, with strong medical terminology and database experience.

Soft Skills fit: They tend to hire detail oriented worker who likes data entry and coding only, not higher level workers. They reject senior candidates who are Clinical Safety Specialists or have higher degrees as overqualified often. English communication skills seem essential. This does not appear to be meant for professional growth. It is meant to only be doing Coordinator and Coding work.