Medical Advisor

Qplus consult bv

Steenokkerzeel

Sur place

EUR 65 000 - 90 000

Plein temps

Il y a 11 jours

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Avantages offerts par ce poste

Health insurance
Meal vouchers
Eco vouchers
Mobility package

Résumé du poste

Qplus consult seeks a Medical Advisor to join our team in Melsbroek (Kalkoven 5, 1820 Steenokkerzeel, Belgium). The role focuses on high-quality scientific information services, medical reviews of adverse events, and PV-related risk management in line with EU legislation.

Required: Medical Doctor degree, 1–3 years in medical advisory/drug safety, on-site 5 days/week, and strong PV knowledge with English at C1/C2. Attractive salary and benefits offered.

Qualifications

  • Master’s degree in Medical Science as Medical physician.
  • 1–3 years of experience as Medical Advisor/Drug Safety Advisor.
  • English level C1/C2; a second EU language is a plus.

Responsabilités

  • Provide first-line scientific and medical information to the PV team and customers.
  • Handle medical review/assessment of medical inquiries and adverse event reports.
  • Perform medical evaluation of adverse reactions and contribute to safety documents.

Connaissances

Medical information
Pharmacovigilance
Scientific communication
English proficiency
Regulatory knowledge

Formation

Master's degree in Medical Science / Medical Doctor

Description du poste

This job is located in Melsbroek (Kalkoven 5, 1820 Steenokkerzeel, Belgium) – please apply only if you live in Belgium and have a valid working permit for Belgium.

Qplus consult offers high-level quality services for pharmaceutical companies. Within the pharmaceutical sector Qplus consult built a solid and strong reputation, therefore we are looking for a motivated, dynamic and flexible Medical Advisor to join our team.

What is the job about?

As a Medical Advisor with Medical Doctor edication degree you focus on providing high quality, comprehensive and scientific information services to our customers regarding their product range. This involves supporting and enhancing the safe and effective use of products, enabling our customers to make informed decisions about their product range.

  • You provide a first line scientific and medical information service to the internal pharmacovigilance (PV) team and customers;
  • You handle Medical Review/Assessment of all medical enquiries, Adverse Event Reports and pregnancy reports, in line with procedures;
  • You take care of a medical evaluation of adverse reactions;
  • You contribute to and perform medical assessments of the specific documents (e.g. safety profile of medicines, detected scientific literature, signals, cases etc.; Periodic and Development Safety reports, Risk Management Plans, DHPC etc.);
  • You provide pharmacovigilance expertise to Risk Management planning cross-functional teams with input to formulation, implementation, maintenance and tracking of local RMPs;
  • You provide a comprehensive information service to external healthcare professionals and patients on the safety of company products in the scope of Risk Minimization Measures;
  • You contribute to the PV audits and inspections as required;
  • As a part of the PV-team, you ensure any drug safety activities are in line and comply with EU-PV-legislation and procedures.
What do we expect from you?
  • You have a Master’s degree in Medical Science as Medical physician;
  • You have a minimum of 1-3 years of experience as a Medical Advisor/ Drug Safety Advisor;
  • You work 5 days per week at our offices (on-site);
  • You have a strong knowledge of PV processes and European PV-legislation;
  • You have a minimum level of C1 or 2 in English, the knowledge of another EU language is a plus;
  • You can work in a fast-moving working environment;
  • You are stress-resistant and work autonomously;
  • You are quality-oriented and meticulous in figuring out and formatting your work;
  • You are result-oriented.
What do we offer?
  • Working at Qplus consult brings new challenges and opportunities every day;
  • You will be part of a dynamic, fast-growing company with a global customer base;
  • Our workplace fosters a healthy environment with fresh fruit, sit-stands desks or desk bikes/treadmills;
  • Attractive and competitive basic salary;
  • Additional benefits like health insurance, meal vouchers, eco vouchers and mobility package;
  • Extensive training and great career growth opportunities.
Who are we?

With our 6 service lines (Medical Affairs, Pharmacovigilance, Quality Management, Regulatory Affairs, Auditing and Training), we are an expert in our job within the pharmaceutical industry.

We emphasise our values: client first, dedication, loyalty, passion, professionalism and performance.

Our main focus is to build a long-term relationship with each of our clients to provide a service of excellence in a timely and cost-efficient manner. To meet these expectations, we have a team of professional experts who are exceptionally highly trained and ready to provide excellent service every day.

Check out our company story here: https://qplusconsult.com/about-qplus-consult/#1533197693393-68307312-4487

and join our team!

Ready to make an impact in the pharmaceutical sector?

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