CRS/Sr. Clinical Research Scientist - USCD&MA CVM (Hypertension)

How do you spend your day? Are you passionate about what you do? At Novartis, our focus is clear, our purpose defined. We're part of a team that's making a difference in the quality of people's lives.
The incumbent will act as the Local Trial Leader at a level commensurate with experience in the implementation and oversight of Phase IV Hypertension studies in the Cardiovascular Therapeutic Area in a group that conducts Phase II-IV clinical trials. Key responsibilities will include interacting with a regionally based field monitoring group in the day-to-day activities of clinical trials, preparation of required study documents (including regulatory documents), and assuring that data is collected according to Novartis Standard Operating Procedures. The incumbent will also interact with other line units in support of clinical trials and ensure that project timelines are met by closely monitoring study activities and resources. Additionally, the CRS/Sr CRS may also assist in the preparation of Clinical Trial Protocols, Clinical Trial Study Reports, publications/manuscripts and may also serve on the clinical trial team. Some travel may be required but is typically less than 10 %. As one of the largest pharmaceutical companies in the world and voted as one of the 100 Best Companies to work for by Working Mother Magazine, we're committed to peak performance, improving the quality of life, and embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive advantage. Novartis is an equal opportunity employer M/F/D/V. PRINCIPALS ONLY!Qualifications
The position will be filled at a level commensurate with experience, however, the requirements include a minimum of a BSN or RN, BA or BS in a scientific discipline, or a pharmacy degree (or equivalent), and at least 3 years of clinical research experience in a pharmaceutical environment. CANDIDATE MUST HAVE AT LEAST TWO YEARS OF DOCUMENTED EXEPERIENCE IN CONDUCTING CLINICAL TRIALS IN A PHARMACEUTICAL ENVIRONMENT. A minimum of five years relevant experience in a clinical research/drug development environment is required for a Sr. CRS position. A background in pharmaceutical industry research in the Cardiovascular area is preferred, but is not required. Effective oral and written communication skills are a must. The demonstrated ability to independently write Clinical Trial Protocols and Clinical Trial Reports is required for a senior level position. The ability to work both independently and collaboratively on Project teams and to recognize safety and efficacy data trends is essential. Knowledge and experience of clinical trial design, analysis, and reporting (for senior positions) is also necessary. The CRS/Sr CRS should be familiar with all aspects of the drug development process and have knowledge of the medical, scientific and clinical research techniques of the assigned area. Working knowledge of GCP and local regulatory requirements is desired.
Novartis is committed to embracing and leveraging diverse backgrounds.
Novartis is an equal opportunity employer M/F/D/V.