Novartis Pharma CDM Job Vacancy 2020 – Apply Online

Novartis Pharma CDM Job Vacancy 2020 – Apply Online

Novartis Pharma CDM, Clinical Data Manager Jobs, Novartis Jobs. Pharmaceutical Science candidates apply online for a Senior Clinical Data Manager position that is available at Novartis. Novartis is hiring Pharma candidates as per the details on the same below:

Job ID 291554BR

Position Title Senior Clinical Data Manager

Eligibility: 

• University or college degree in life science, computer science, pharmacy, nursing or equivalent relevant degree
• Two or more years of experience in drug development with at least 2 years of experience in Data Management.
• Understanding of clinical trial methodology, GCP and medical terminology
•  Good organizational and project management skills. Intermediate presentation and problem-solving skills
•  Good communication and interpersonal skills. Excellent written and oral English skills
• Ability to work well in a team.May coordinate and provide direction on task to other data management team members

Responsibilities:

• Serve as Project Data Manager for multiple projects/trials from multiple business units (BUs) and providing professional Data Management input to Clinical Trial Teams (CTTs). Responsible for ensuring consistency of protocols, project CRFs, clinical databases for all trials within assigned projects and provide technical feedback to CROs as needed.
• Provide CDM input to study protocols and Study Specification Worksheets (SSW) for CRO proposal requests; audit/qualify CROs at India and provide input on CRO selection. Develop CDM presentations for Investigator Meetings, CRA workshops, and Project Kick-off meetings, and Validation and Analysis Plans (VAPs) as appropriate.
• Ensure complete and consistent medical term coding using appropriate standard dictionaries; ensure consistency of serious adverse event data across clinical and drug safety databases.
• • Monitor clinical data quality and progress of trials outsourced to international CROs; drive corrective actions as needed; ensure proper integration of third-party/non-CRF data as applicable. Proactively identify project threats and resolve issues with clinical trial teams; escalate to US Biometrics management if necessary and appropriate.

Apply Online

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