SIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!Our client is a professional Pharmaceutical and Biotechnology organisation, based in Vlaams-Brabant Belgium.

The Company

Janssen develops treatments for some of the most devastating disorders and complex medical challenges of our times, including cancer, hepatitis, HIV/AIDS, diabetes, arthritis, dementia, and mental disorders. We focus our research on six strategic pathological areas: oncology, neurosciences, infectious diseases and vaccines, immunology, cardiovascular and metabolic disorders and pulmonary hypertension .

Role Description

The responsibilities of the Clinical Research Manager follow the Early Development & Clinical Pharmacology Hybrid Trial Oversight Model, effective as of 15th of September 2013. You provide guidance and leadership to representatives of various functional areas involved in the initiation, conduct, execution and finalization of Phase-0, Early-Development and Phase IIa studies. You keep total oversight of the end-to end activities, from writing of protocol synopsis to reviewing Clinical Research Reports, for the Phase 0, Early Development and Phase IIa studies.

Responsibilities

- You are a full member of the Early Development Disease Clinical Team (Phase 0, ED, Phase lla)
- You lead the Clinical Working Group
- You develop the study documents

Requirements

- University Degree (Bachelor, Master PhD);
- Experience in the medical or paramedical (pharmacy, biology, veterinary, etc.) field;
- Experience with clinical development (clinical study monitoring, clinical study management, etc.);
- Knowledge of Hepatitis, Respiratory Diseases and/or Infectious Diseases in general
- Team Work experience;
- Experience of working in a matrix-structured organisation is a plus;

Other information

This is a short summary of the position. For the full job description, send me a request to c.roffelsen@sire-search.com.

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Cees Roffelsen.