Your Responsibilities :
This role gives YOU the opportunity to lead key activities to progress YOUR career, the main of this is to lead role for within-
country operational feasibility, planning and delivery of Phase I-IV clinical trials and epidemiological and Health Outcome studies in a specific country or cluster of countries.
They are accountable for within-country execution and delivery of assigned studies to time, budget and quality expectations as defined in the clinical development plan and study protocol as well as in local regulations, IND / GCP / ICH-
guidelines, GSK Corporate, Vaccines, and local SOPS and POLs. Their scope of work includes matrix leadership and project management of country and site-
level activities including site management & monitoring activities within their assigned countries. The LDL serves as the operational point-
of-contact between the central Study Delivery Lead and in-country operational staff aligned to study.
In all geographies it is recognized that the LDL is part of the local GSK community and collaborates closely with local medical staff (who are responsible for local medical and scientific elements of the study) as well as with Clinical Research Associates (CRA) / monitors and other in-country staff.
Basic qualifications :
We are looking for professionals with these characteristics to achieve our goals :
This role requires a good understanding of scientific and medical information and an ability to apply this understanding to the conduct, management and oversight of clinical research activities.
Main capabilities :
comfortable projecting, managing, and reporting budget information (business and financial acumen)
Preferred qualifications :
However, if you have the following
Given the nature of the job, the associated responsibility, the need to coordinate multi-disciplinary teams in the development of a research trial, a good scientific or clinical background associated with operational skills is preferred.
These roles interface directly with external physician and other clinical site staff and must be able to intelligently convey GSK positions and requirements to a highly educated external partner group.
If you feel this is your next career move, please apply up to August 22, 2018
Why GSK? :
We are a science-led global healthcare company with a special purpose : to help people do more, feel better, live longer.
We have 3 global businesses that research, develop and manufacture innovative pharmaceutical medicines, vaccines and consumer healthcare products, including Sensodyne, CataflamPro / Voltaren, Theraflu / Trimedal, Parodontax, Panadol.
In over 150 countries and 300 years of history, our goal is to be one of the world’s most innovative, best performing and trusted healthcare companies to bring differentiated high-
quality and needed healthcare products to as many people as possible, with our scientific and technical know-how and talented people.
As a GSK Employee, you will put our values and expectations at the heart of everything you do. You will have the courage to make decisions, taking the accountability for them, guided by our strategy, priorities and values of patient focus, respect for people, integrity and transparency.
Being a GSK employee allows you to challenge and to change by ensuring your development meet changing business needs. You will also enjoy to be part of a diverse team, getting inspired by our teamwork, our healthy and inclusive environment and specially by making the difference and playing an important role on the benefit of millions of patients and consumer worldwide.
Our inclusive workplace makes our employees feel engaged by the contribution they make, by affording them equal treatment regardless of actual or perceived characteristics.
As so, when you apply for a job at GSK, it is not necessary to include on your resume information such as : race, color, ethnicity, age, gender, sexual orientation, marital status, religion, origin, photographs or any other personal characteristics.
Find out what life at GSK is really like www.gsk.com
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