Remote Clinical Trial Manager — End-to-End Study Lead

BMS; Lawrence Township (NJ); On-site; USD 104,000 - 125,000; Full time

Benefits offered by this job

Flexible Time Off

11 Paid Holidays

Comprehensive benefits

Job summary

Bristol-Myers Squibb Co is seeking a Clinical Trial Manager to oversee end-to-end study delivery at the country level, aligning timelines, budgets, and quality with global study teams. The CTM will coordinate with local cross-functional teams, drive country feasibility, patient recruitment, and data integrity in CTMS/eTMF, while supporting regulatory submissions and site interactions.

The role requires collaboration, risk management, and occasional local travel to ensure milestones are met, with

Qualifications

• Bachelor's or Master's in life sciences; required.
• Minimum of 4 years' industry experience.
• Experience leading cross-functional teams.
• SME in areas with regional/global impact.
• Willingness to travel locally < 1 month/quarter.

Responsibilities

• Act as country study lead with global teams and coordinate with local cross-functional teams.
• Implement country feasibility and targets as endorsed by country leadership.
• Plan, develop and execute timelines for start-up with GTAC and stakeholders.
• Lead country/site-level patient recruitment strategy and risk mitigation.
• Ensure CTMS/eDC/eTMF data integrity and access for country/site personnel.
• Support regulatory submissions and ethics submissions where applicable.

Skills

GCP & ICH

Clinical research processes

Cross-functional teamwork

Communication skills

English + local language

Education

Bachelor's or Master's in life sciences

Tools

CTMS

eDC

eTMF

Microsoft Suite

Job description

Bristol-Myers Squibb Co is seeking a Clinical Trial Manager to oversee end-to-end study delivery at the country level, aligning timelines, budgets, and quality with global study teams. The CTM will coordinate with local cross-functional teams, drive country feasibility, patient recruitment, and data integrity in CTMS/eTMF, while supporting regulatory submissions and site interactions.

The role requires collaboration, risk management, and occasional local travel to ensure milestones are met, with