Junior Consultant - Pharma

KAMPENHOUT (OTHER)HYBRIDPOSTED: 6/24/2026
PHARMAFull-time
HIRING ORGANIZATIONIQVIAHealthcare Technology & Contract Research
Iqvia

ROLE DEFINITION & RESPONSIBILITIES

We are looking for a Junior Consultant to join our team.

Main Areas of Responsibility

As a junior consultant at IN2Pharma, you will be trained to support more senior colleagues in ensuring the client’s products meet the required standards of quality and safety and in ensuring regulatory compliance for a defined range of products of the client’s portfolio. This gives you the opportunity to acquire experience within one or several of the following domains:

Medical & Regulatory Affairs

Medical writing: expert reports, clinical evaluations, literature study

Medical education of sales representatives: product training on medicinal or healthcare products

Review and approve promotional material for medicinal and healthcare products

Adapt SPC, PIL and packaging materials in line with the registration file and legislation

Pharmacovigilance (PV)

Local Literature Review for adverse events on the MAH’s medicinal products

Assist in the PV quality system set-up or maintenance: PV SOPs, gap analysis, compliance check with applicable regulations

Training of MAH’s employees in PV awareness

Quality Assurance (QA)

Support the QP/RP in all aspects related to quality and compliance ensuring local requirements are met

Support the QP/RP in the administrative release to the market in compliance with procedures. This includes: QA check, CoA request, Artwork request, Contact with warehouse/supply,…

Investigate customer complaints and non-conformance issues

Technical Skill Requirements

Master degree in life sciences

Good knowledge of national and European regulations and legislations for medicinal products

Good communication skills in Dutch, French and English (both verbal and written)

Strong initiative, problem solver and good organizational skills

Accurate & efficient: concern for quality, compliance and consistency

Good communicator & team player

Our offer

A permanent full-time position with a competitive package and supplementary benefits

Challenging and alternating job as consultant within a dynamic team

Development opportunities by working on various projects for different pharmaceutical companies

IN2Pharma is a consulting company passionate about offering solutions in Medical, Regulatory Affairs and Quality Assurance projects for pharmaceutical and healthcare industry in Benelux. Our offices are located in Kampenhout at the business center “Hof ter Loonst”.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

REQUIRED VERIFIED SKILLS

Regulatory Affairs
Pharmacovigilance
Medical Writing
Clinical Research
Quality Assurance

COMPENSATION & REWARDS

Salary: Competitive / Disclosed upon candidate shortlisting
Salary for this Junior Consultant - Pharma position is competitive and aligned with industry standards for this location.

ORGANIZATION CONTEXT & CULTURE

IQVIA is a leading global provider of advanced analytics, technology solutions, and contract research services (CRO) to the life sciences industry. The company helps pharmaceutical, biotech, and medical device clients accelerate the development and commercialization of new medical treatments through its extensive data, technology, and human expertise. Their offerings span from clinical trial design and execution to real-world evidence and commercial effectiveness.

TEAM SIZE: 87,000+ employees
INDUSTRY: Healthcare Technology & Contract Research

EXPECTED CAREER ROADMAP

Career path typically progresses from Associate, to Senior Specialist, and eventually to Manager or Lead positions within the department.

APPLICATION ADVISORY

Ensure your resume clearly showcases experience with: Regulatory Affairs, Pharmacovigilance, Medical Writing. Prepare real-world examples demonstrating these skills for the interview.

READY TO SUBMIT?

Verify your capability profile and matching credentials before submitting direct applications.