Highlights
Preliminary evaluation of clinical trial, spontaneous (post-marketing), and solicited reports of adverse events, including communication with partners and affiliates when necessary to verify completeness and accuracy. Receipt and triage of adverse event reports for marketed and investigational products from all sources.
Numbers & Facts
| Location | Nutley, NJ (Remote) |
| Industry | Staffing/Employment Agencies |
| Salary | $28.57 |
| Company Size | 2,000 to 2,499 employees |
| Year Founded | 2000 |
| Website | http://www.lancesoft.com/ |
Description
100% remote
Receipt and triage of adverse event reports for marketed and investigational products from all sources. Preliminary evaluation of clinical trial, spontaneous (post-marketing), and solicited reports of adverse events, including communication with partners and affiliates when necessary to verify completeness and accuracy.
Case preparation - duplicate searches, initial data entry, and assignment of cases to Specialists. Particular emphasis is placed on determination of seriousness, expectedness, and validity. Prioritizes workload to ensure Company and Regulatory Authority deadlines are met. May include internal and external distribution of information to co-marketing partners, and others as requested.
Requirements:
Bachelor s degree required, preferably in a scientific or medical discipline
Previous experience in data coding and retrieval skills using database technology
Knowledge of medical terminology
Prior work experience in Product Safety/Pharmacovigilance preferred
Precise attention to detail and ability to multi-task
Good communication skills, both written and verbal
Ability to work independently, and as part of a team
Note: This position is remote, Mon-Fri (7.5 hours/day).
Looking for less than 7 years experience.
Not looking for advanced degree.
Receipt and triage of adverse event reports for marketed and investigational products from all sources. Preliminary evaluation of clinical trial, spontaneous (post-marketing), and solicited reports of adverse events, including communication with partners and affiliates when necessary to verify completeness and accuracy.
Case preparation - duplicate searches, initial data entry, and assignment of cases to Specialists. Particular emphasis is placed on determination of seriousness, expectedness, and validity. Prioritizes workload to ensure Company and Regulatory Authority deadlines are met. May include internal and external distribution of information to co-marketing partners, and others as requested.
Requirements:
Bachelor s degree required, preferably in a scientific or medical discipline
Previous experience in data coding and retrieval skills using database technology
Knowledge of medical terminology
Prior work experience in Product Safety/Pharmacovigilance preferred
Precise attention to detail and ability to multi-task
Good communication skills, both written and verbal
Ability to work independently, and as part of a team
Note: This position is remote, Mon-Fri (7.5 hours/day).
Looking for less than 7 years experience.
Not looking for advanced degree.
About Company
We are a $125 Million, NMSDC-certified Minority & Woman owned Workforce Solutions Company headquartered in the DC metro area with presence across US with global presence - Canada, Mexico, India, UK, Malaysia, Indonasia, Hongkong, Singapore, UAE. We are specialized in providing Workforce Solutions, SOW project delivery, Engineering Solutions, Creative Services. We currently support 100+ Fortune companies globally and across multiple industry segments. We are currently supporting several massive programs across industry segment nationally/globally (Intel, Ally, AMD, QUALCOMM, Morgan Stanley, Kraft/ Mondelez, MNP, Amdocs, Dell, SanDisk, Medtronic, Becton Dickinson, GE, Lockheed Martin, UTC, L-3 Communications, Caterpillar, BMW, Mercedes Benz, National Grid, Dominion, Energy Future Holdings, PSEG, 3M, Fidelity, Aetna, Humana, Johnson & Johnson, Pfizer, Merck etc).
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender, identity, national origin, disability, or protected veteran status.