Skip to main content
PrimeVigilance

PV Officer- Senior PV Officer, Team Leader (Pharmacovigilance Manager)

RemoteRomania only
Published
Experience
Senior
Employment
Full-time
Salary not disclosed
Check eligibility

Open to RO only. Set where you work from to check your eligibility.

No BS summary

Pharmacovigilance professional with 3-4 years of experience, including at least 1 year in a line management role. Requires excellent communication, organization, delegation, planning, and time management skills, fluency in English, and advanced MS Office literacy. Life science or healthcare-related degree is preferred.

Required skills

MS Office

Required languages

English fluent

What you'll do

  • Providing support to other activities undertaken by the project team on behalf of the client and the company
  • Line Manages assigned ICSR staff
  • Creates and maintains project specific KPIs for contracted ICSR activities (this includes optimizing procedures, trainings and any other actions to increase ICSR team efficiency)
  • Proposes process changes to ICSR Operational Lead
  • Manages ICSR deviations with ICSR Operational Lead support
  • Reviews trackers and timesheet data and ensures accuracy
  • Is involved in ICSR processing and 2nd QC of cases
  • Support other departments, as approved and instructed by ICSR Operational Lead
  • Operates as the assigned team SME
  • Supporting the RA & PV Network Department as needed, including acting as the LCPPV (Local Contact Person for Pharmacovigilance) for the specified country and taking on the role of PRLS (Person Responsible for Local Screening) for the designated language, as agreed with the line manager

What they require

  • Life science graduate, pharmacy, nursing, other healthcare related qualification or experience in pharmacovigilance
  • 3-4 years of work experience in pharmacovigilance within which minimum 1 year of work experience in line manager role.
  • Excellent communication (written and verbal) skills
  • Organization skills, including attention to details and multitasking
  • Delegation skills
  • Planning and time management
  • Technical skills
  • Team working
  • English – fluent (spoken, written)
  • Advanced literacy (MS Office)

Benefits

  • Medicine moves forward here. So will you.
  • patient safety is not one part of the job. It is why we exist.
  • Keeping patient safety at the center of every decision, from early development through to post-marketing surveillance.
  • spotting the signal that matters early and turning it into insight our clients can act on.
  • a culture worth staying for.
  • an environment built on kindness, flexibility, growth and belonging, where colleagues support one another and good ideas are heard wherever they come from.
  • a role with real purpose, global reach and the chance to keep growing while you help protect patients, you will feel at home here.
  • When you join Ergomed Group, you make a difference by helping to bring safe and effective pharmaceutical treatment to patients around the world.
  • You’ll join a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting.
  • We are diverse in many ways, yet our values unite us.
  • Quality: we hold ourselves to the standard patients deserve.
  • Integrity and trust: we do the right thing, especially when it is hard.
  • Drive and passion: we care about the outcome, because someone is waiting on it.
  • Agility and responsiveness: we move quickly, because patients cannot wait.
  • Belonging: everyone is welcome, and every voice counts.
  • Collaborative partnerships: we go further by going together.

PrimeVigilance is a global pharmacovigilance specialist helping clients navigate complex regulations and patient safety from early development through post-marketing surveillance.

PharmaceuticalsMid-size

What people say about this company

2.5/ 5

Salary not disclosed