Senior Clinical Research Associate
Novartis
July 02, 2026
Remote friendly (United States)
United States
Clinical Research and Development
Key Responsibilities
- Lead assigned sites as the primary point of contact throughout study delivery.
- Build strong relationships to ensure site performance, quality, and milestone achievement.
- Manage Phase I to Phase IV trials per monitoring plans and company procedures.
- Conduct site initiation visits and provide ongoing training for site personnel.
- Perform remote and on-site monitoring to ensure compliance and patient safety.
- Maintain accurate documentation and update clinical systems in a timely manner.
- Identify risks, resolve issues, and escalate concerns as needed.
- Collaborate with cross-functional teams to drive efficient study execution.
- Support timely data query resolution and ensure data accuracy.
- Act as a subject matter expert across study activities when required.
Essential Requirements
- Minimum of three years of clinical site monitoring experience.
- Bachelor’s degree in science, healthcare, or related field.
- Strong understanding of clinical research and drug development processes.
- Knowledge of ICH/GCP.
- Ability to manage multiple priorities and work independently.
- Strong site management, communication, and problem-solving skills.
- Fluency in written and spoken English.
- Ability to travel extensively (domestic and international).
Desirable Requirements
- Experience in radioligand therapy, CAR T-cell therapy, or oncology.
- Preference for location in VA, DC, MD, DE, PA, or NJ.
Role/Work Details
- Remote-based anywhere in the U.S. (no relocation).
- 80% travel required.
Benefits/Compensation
- Salary expected to range from $108,500 to $201,500 per year; performance-based cash incentive; potential eligibility for annual equity awards; comprehensive benefits package and time off.
Application Instructions
- Not specified.
- Lead assigned sites as the primary point of contact throughout study delivery.
- Build strong relationships to ensure site performance, quality, and milestone achievement.
- Manage Phase I to Phase IV trials per monitoring plans and company procedures.
- Conduct site initiation visits and provide ongoing training for site personnel.
- Perform remote and on-site monitoring to ensure compliance and patient safety.
- Maintain accurate documentation and update clinical systems in a timely manner.
- Identify risks, resolve issues, and escalate concerns as needed.
- Collaborate with cross-functional teams to drive efficient study execution.
- Support timely data query resolution and ensure data accuracy.
- Act as a subject matter expert across study activities when required.
Essential Requirements
- Minimum of three years of clinical site monitoring experience.
- Bachelor’s degree in science, healthcare, or related field.
- Strong understanding of clinical research and drug development processes.
- Knowledge of ICH/GCP.
- Ability to manage multiple priorities and work independently.
- Strong site management, communication, and problem-solving skills.
- Fluency in written and spoken English.
- Ability to travel extensively (domestic and international).
Desirable Requirements
- Experience in radioligand therapy, CAR T-cell therapy, or oncology.
- Preference for location in VA, DC, MD, DE, PA, or NJ.
Role/Work Details
- Remote-based anywhere in the U.S. (no relocation).
- 80% travel required.
Benefits/Compensation
- Salary expected to range from $108,500 to $201,500 per year; performance-based cash incentive; potential eligibility for annual equity awards; comprehensive benefits package and time off.
Application Instructions
- Not specified.