Clinical Research & Development Lead (CRDL) Th HBV

Are you energized by the opportunity to partner with key leaders in global clinical development and to accelerate business performance and drive global operational support?

If so, this Clinical Research Development Lead, Director (CRDL) Therapeutic role could be an ideal opportunity for you.

This position will be based in Belgium.

The CRDL Therapeutic conducts Phase I-IV Clinical Development activities within a large program or group of related programs (led by a Clinical and Epidemiology Research & Development Project Lead - CEPL) or, for a mid-size program, to lead Clinical Development activities within the context of the GSK Vaccines process in order to ensure the high quality and on-time delivery of all clinical data that will allow world-wide registration in compliance with the clinical development plan, good clinical practices (GCP), and GSK Vaccines standard operating procedures (SOP).

Your responsibilities:

• You participate in Clinical Development activities for a series of studies within a large program or group of related programs or, for a mid-size program, lead Clinical Development activities.
• You serve as a scientific and management reference for the project (internally/externally)
• You are responsible for budget, resourcing and timing: you support the clinical team to consistently achieve high standards in attainment of project timelines in global programs.
• You provide support to Marketing/Business Development throughout product life cycle
• You actively follow-up the product-related Environment

Basic Qualifications:

We are looking for professionals with these required skills to achieve our goals:

• Medical Doctor degree
• Min 1 years’ experience in pharmaceutical industry is required, specifically in Drug Development.
• Excellent knowledge of spoken and written English
• Good theoretical and practical knowledge in clinical research.
• ability to translate scientific skills in the field of vaccines and clinical research into business-driven strategies.
• Ability to work well within a matrix environment, balance priorities, and handle multiple tasks through good planning, project administration, and organization skills.
• Effective ability to prioritize tasks and deliver on deadlines, with high performance standards and a commitment to excellence.
• Strategic thinking skills and achievement oriented.
• Able to critically analyze information, identify strengths and weaknesses of approaches and develop remedial actions to mitigate risks.
• Ability to understand high level corporate and business objectives: rapid, flexible, innovative working and decision making
• Needs to possess highly effective communication skills and be capable of presenting ideas and data clearly to various audiences.

Preferred Qualifications:

If you have the following characteristics it would be a plus:

• Previous experience in the field of pediatrics, obstetrics and gynecology, infectious diseases, clinical epidemiology, pharmacoepidemiology, and/or clinical vaccinology is an asset
• Previous vaccinology experience highly desirable
• Understanding of GCP and ICH guidelines; experience working with Regulatory functions (i.e. filing IND, BLA, CTD) is a plus
• Sensitivity to the needs of a diversified ethnic groups and ability to build rapport across the spectrum
• License to practice medicine and board and/ or professional certification is an asset

Basic Qualifications:

We are looking for professionals with these required skills to achieve our goals:

• Bachelor’s degree
• Experience implementing technical solutions in a clinical data management setting
• Experience translating clinical protocols into technical specifications
• Experience managing data quality, safety, risk management & regulatory guidelines

Preferred Qualifications:

If you have the following characteristics, it would be a plus:

• Master’s degree
• Understanding of relevant R&D processes and objectives
• Proven project management skills to lead and manage change projects

At GSK, we have already delivered unprecedented change over the past four years, improving R&D, becoming a leader in Consumer Healthcare, strengthening our leadership, and transforming our commercial execution. Now, we’re making the most significant changes we’ve made to our business in over 20 years. We’re on track to separate and create two new companies in 2022: New GSK with a leading portfolio of vaccines and specialty medicines as well as R&D based on immune system and genetics science; and a new world-leading consumer healthcare company of loved and trusted brands.

With new ambition comes new purpose. For New GSK, this is to unite science, talent, and technology to get ahead of disease together – all with the clear ambition of delivering human health impact; stronger and more sustainable shareholder returns; and as a new GSK where outstanding people thrive.

Getting ahead means preventing disease as well as treating it. How we do all this is through our people and our culture. A culture that is ambitious for patients – so we deliver what matters better and faster; accountable for impact – with clear ownership of goals and support to succeed; and where we do the right thing. So, if you’re ready to improve the lives of billions, join us at this exciting moment in our journey. Join our challenge to get Ahead Together."

• Li-GSK

If you have a disability and require assistance during the course of the selection process, you will have the opportunity to let us know what specific assistance you require in order to make suitable arrangements.

Our goal is to be one of the world’s most innovative, best performing and trusted healthcare companies. We believe that we all bring something unique to GSK and when we combine our knowledge, experiences and styles together, the impact is incredible. Come join our adventure at GSK where you will be inspired to do your best work for our patients and consumers. A place where you can be you, feel good and keep growing.

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