Senior Clinical Research Associate

October 9

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Novartis

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Cardiovascular • Immunology • Neuroscience • Solid Tumors • Hematology

10,000+

Description

• Remote Position covering Eastern US • Required to travel up to 80% of the time • Performs monitoring activities related to Phase I-IV Oncology and Pharma clinical trials • Responsible for delivering data within timelines and quality standards • Serves as the primary site manager for assigned clinical investigative sites • Ensures compliance with protocol and regulations to secure data integrity and patient safety • Collaborates with internal stakeholders for data query resolution and seamless site management

Requirements

• BS/BA degree. Scientific or healthcare discipline preferred • Minimum of 3 years’ experience in site monitoring strongly preferred • Excellent knowledge of the drug development process specifically clinical trial/research • Knowledge of international standards (GCP/ICH, FDA, EMEA) • Ability to manage multiple priorities and manage time efficiently • Excellent Site management capabilities with demonstrated negotiating and problem-solving skills • Strong communicator and presentation skills (oral and written) • Fluent in both written and spoken English

Benefits

• Full range of medical benefits • Financial benefits (401(k) eligibility) • Paid time off benefits (vacation, sick time, parental leave) • Potential for sign-on bonus • Restricted stock units and discretionary awards