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BusinessOperations - Pharmacovigilance Specialist I - 590202

Role overview

Qualifications

  • High school diploma or equivalent
  • 1+ years of pharmaceutical or healthcare related work experience
  • Proficient with Microsoft Office Suite (Outlook, Word, Excel)
  • Associate’s degree preferred

Responsibilities

  • Collecting, monitoring, processing, and distributing adverse event reports and information queries
  • Prepare and submit adverse event cases to pharma clients or FDA
  • Reviews safety and medical information for assigned products
  • Prepares and mails time sensitive documentation for processing adverse event cases

Key facts

Hard skills

Other skills

  • Microsoft Office
  • Detail Oriented
  • Communication
  • Prioritization
  • Multitasking

About the company

Mindlance logo

Mindlance

Staffing & Recruiting

Founded in 1999, Mindlance is one of the largest diversity-owned staffing firms in the US and has been on SIA’s list of Fastest Growing US Staffing Firms for 10 years. Mindlance has also been recognized as one of the consistently best performing partners to industry-leading MSP programs including Allegis, Kelly, TAPFIN, PROUnlimited, Pontoon, GRI, WorkforceLogiq and Agile-1.What started with contingent staffing has developed to a comprehensive portfolio of workforce solutions. Along with industry specific, talent-centric staffing across a range of specializations- Technology, Engineering, Scientific, Clinical Research, Digital, Creative, Marketing, Profession, Mindlance provides Managed Recruitment services- RPO and Direct + Diverse Sourcing, and Pay+ Services- EoR/Payroll, IC Compliance and AoR.Mindlance is also generating alternative talent pipelines that prioritize diversity through three Diverse Talent Acceleration offerings: (1) RebootTalent, a diverse returning talent acceleration service (2) Mindlance Diversphere, a private diverse talent pool aggregated from a network of diversity partnerships and (3) Quintrix Solutions, an upskilling recruit-train-deploy service.With a year-over-year growth rate of 20% and an annual revenue of over $400 million and growing, the Mindlance story is one of calculable achievement, made meaningful by the commitment to grow a mindful way that creates balance in the work and societal ecosystem.Visit www.mindlance.com to learn more about us and our latest job openings.STAFFING INDUSTRY ANALYSTS RECOGNITIONS:Fastest Growing U.S. Staffing Firms (2022, 2021, 2019, 2018, 2017, 2016, 2015, 2014, 2013, 2012, 2011)Largest U.S. Staffing Firms (2022, 2021, 2020, 2019, 2018, 2017, 2016, 2015)Largest Diversity-Owned U.S. Staffing Firms (2022, 2021, 2020, 2019, 2018, 2017, 2016, 2015)Largest IT Staffing Firms (2022, 2021, 2020, 2019, 2018, 2017)Largest Clinical & Scientific Staffing Firms (2022, 2021, 2020, 2019, 2018, 2017)

Company details

Company typeLarge
IndustryStaffing & Recruiting
Company size1001 - 5000

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Job description

Position Purpose: Monitor and report any adverse events or side effects of pharmaceutical products on the market. Report adverse reactions and product complaints received from healthcare professionals and consumers.

Education/Experience:
High school diploma or equivalent. Associate’s degree preferred. 1+ years of pharmaceutical or healthcare related work experience. Medical assistance or project coordination experience preferred. Experience or basic knowledge of adverse events preferred. Proficient with Microsoft Office Suite (Outlook, Word, Excel).

Responsible for collecting, monitoring, processing, and distributing adverse event reports and information queries
Prepare and submit adverse event cases to pharma clients or FDA
Reviews safety and medical information for the assigned products, including safety components of protocols and studies for assigned drugs
Prepares and mails time sensitive documentation necessary for the processing of adverse event cases

EEO:

“Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of – Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.”

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Position Purpose: Monitor and report any adverse events or side effects of pharmaceutical products on the market. Report adverse reactions and product complaints received from healthcare professionals and consumers.

Education/Experience:
High school diploma or equivalent. Associate’s degree preferred. 1+ years of pharmaceutical or healthcare related work experience. Medical assistance or project coordination experience preferred. Experience or basic knowledge of adverse events preferred. Proficient with Microsoft Office Suite (Outlook, Word, Excel)." "Responsible for collecting, monitoring, processing, and distributing adverse event reports and information queries
Prepare and submit adverse event cases to pharma clients or FDA
Reviews safety and medical information for the assigned products, including safety components of protocols and studies for assigned drugs
Prepares and mails time sensitive documentation necessary for the processing of adverse event cases"
Story Behind the Need
  • What is the purpose of this team?
  • Describe the surrounding team (team culture, work environment, etc.) & key projects.


We are a very small team who work very close with one another and try to make all feel welcome.
Data input and manipulation using ScriptMed and Microsoft word, Excel, and PDF. Training
  • Describe the training this worker will complete (length of training, nesting, etc.).
  • What are the training requirements (time off, alternate schedule, etc.)?
Training is 4-8 weeks
most time is going to be spent shadowing a team member on actual tasks. Typical Day in the Role
  • Walk me through the day-to-day responsibilities and a description of the project (Outside of the Workday JD).
  • What are the performance expectations/metrics?
User will process AE documents each day based on assignments from shared excel log. These will be sent via email. A lot of Data entry.
Performance expectation is completion of 33 reports per 8 hour day. Candidate Requirements Education/Certification Required: high school diploma Preferred: NA Licensure Required: NA Preferred: NA
  • Years of experience required
  • Disqualifiers
  • Additional qualities
Years of experience required- 1+ years of pharmaceutical or healthcare related work experience

Disqualifiers: not being proficient in Microsoft office

Additional qualities to look for: Proficient with Microsoft Office Suite (Outlook, Word, Excel) Strong verbal, written, and interpersonal communication skills. Strong organization and prioritization skills; ability to multitask, Excellent attention to detail,
  • Top 3 must-have hard skills stack-ranked by importance
1 Basic computer knowledge and computer keyboarding skills 2 Proficient with Microsoft Office Suite (Outlook, Word, Excel) 3 Excellent attention to detail Candidate Review & Selection
  • Shortlisting process
  • Second touchpoint for feedback
  • Candidate review & selection
  • Interview information
  • Onboard process and expectations
Projected Manager Candidate Review Date: ASAP
Type of Interviews:
teams – camera on Required Testing or Assessment (by Vendor): NA Next Steps
  • Additional background check requirements (List DFPS or other specialty checks here):
NA
  • Do you have any upcoming PTO?
  • Colleagues to cc/delegate:

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MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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