Clinical Study Administrator

Job description

LEARN TO SEE THINGS DIFFERENTLY AND APPLY TO BE A :

Clinical Study Administrator

Are you inquisitive, self-driven and highly motivated? Will you make a difference to our company and your colleagues around you by encouraging collaboration? If the answer is yes, then we'd like to hear from you. We are looking for a passionate individual with High School Diploma or equivalent (a Diploma in the field of Clinical Research, e.g. CRA or similar, is an advantage) and a substantial experience in the field of clinical study conduct (within CROs, Pharmaceutical, Biotech, Medical Device industry), including experience in Quality Control of clinical study documentation. You previously worked in management of Study Master Files and archiving of clinical documentation. You also have a good knowledge of ICH GCP, are fluent in English (knowledge of any other languages is an asset) and you possess a good knowledge of MS Office Suite.

RISE TO THE CHALLENGE

Philip Morris Products S.A. is seeking a talented professional to join our Clinical Assessment team (within Clinical Operations, in Research & Development), based in Neuchâtel – Switzerland, whose objective is to support the development and assessment of new products with the potential to reduce the risks* of smoking-related diseases. You will support Clinical Operations team during preparation, execution and reporting of clinical studies.

Additional responsibilities :

- Organize and participate in Clinical Study Team meetings, Investigator Meetings and other relevant events including preparation of agenda/minutes and distribution of documentation as necessary

- Set-up, maintain and archive paper and electronic Study Master File (SMF), as well as ensure completeness of SMF at the end of the studies

- Act as Clinical Administrator of the electronic document management system (R2D2) and provide support to Clinical Study teams

- Maintain existing templates for clinical documents, coordinate development of new templates and ensure edition/quality control of the templates in R2D2

- Provide support to the preparation and maintenance of the GCP training program and records for the PASS team

- Track and check all invoices related to clinical study contracts

- Provide support to the Clinical Assessment Group and Study Teams

- Provide guidance and oversee daily activities of junior contracted study administrator(s)

- Perform Quality Control checks of selected study documents

- Stay up to date with ICH GCP knowledge

FIND A NEW PATH

Our company offers you a new and fresh scientific perspective. Here, you will never stop exploring and discovering. We take on-the-job learning to another level, giving you every opportunity to develop your career and reach your fullest potential. This position will advance your experience with innovative technologies in a highly dynamic environment. Backed by a competitive salary and compensation package, you will work in a professional setting with clients and team members from all over the world.

JOIN A GLOBAL MARKET LEADER

Philip Morris International Inc. (PMI) is the leading international tobacco company, with six of the world's top 15 international brands, including the number one cigarette brand worldwide. PMI's products are sold in more than 180 markets. In 2014, the company held an estimated 15.6% share of the total international cigarette market outside of the U.S., or 28.6% excluding the People's Republic of China and the U.S. PMI is an Equal Opportunity Employer. For more information, see www.pmi.com .

If you wish to contribute to the future of our business and to the new scientific journey of the industry, please apply online.

A valid Swiss work permit or Swiss or EU-25/EFTA citizenship is required for this position.

* Reduced Risk Products (“RRPs”) is the term we use to refer to products with the potential to reduce individual risk and population harm in comparison to smoking combustible cigarettes. PMI's RRPs are in various stages of development, and we are conducting extensive and rigorous scientific studies to determine whether we can support claims for such products of reduced exposure to harmful and potentially harmful constituents in smoke, and ultimately claims of reduced disease risk, when compared to smoking combustible cigarettes. Before making any such claims, we will rigorously evaluate the full set of data from the relevant scientific studies to determine whether they substantiate reduced exposure or risk. Any such claims may also be subject to government review and approval, as is the case in the USA today.

PMI affiliates do not accept referrals from employment agencies in respect of the vacancies posted on this site. Should an employment agency take any action in respect of such a vacancy, their actions will have been taken without the request or agreement of any PMI affiliate. No PMI affiliate shall be liable for any fees in such circumstances.