Global Director, Clinical Project Management
About The Position
SystImmune is seeking a highly skilled and motivated Global Director, Clinical Project Management (CPM) to join their dynamic team. The successful candidate will oversee and coordinate global clinical trials from initiation through to completion. This role involves ensuring compliance with regulatory requirements, managing study timelines and budgets, and fostering effective communication among stakeholders. The global Director, Clinical Project Management will play a critical role in delivering high-quality data and ensuring the success of clinical studies. This position requires onsite hybrid work model in Princeton, NJ.
Requirements
- Bachelor’s degree in Life Sciences, Nursing, or a related field.
- Minimum of 10 years of experience in clinical trial management, including at least 5 years in a direct line management role.
- Strong understanding of GCP and regulatory requirements.
- Excellent organizational and project management skills.
- Proven ability to lead cross-functional teams and manage multiple priorities.
- Strong communication and interpersonal skills.
- Ability to work collaboratively in a team-oriented environment
- Flexibility and adaptability to changing priorities and workload
Nice To Haves
- Master’s degree in a related field or clinical research certification (e.g., ACRP or SOCRA).
- Experience with electronic data capture (EDC) systems and clinical trial management software.
- Prior experience in running or supporting Oncology clinical trials a plus.
- Previous experience in a sponsor or CRO environment.
Responsibilities
- Oversee the planning and execution of global clinical trials
- Develop and implement study protocols, timelines, and budgets.
- Manage all aspects of clinical trial operations, including site selection, initiation, monitoring, and closeout.
- Ensure compliance with Good Clinical Practice (GCP) and regulatory guidelines.
- Coordinate with cross-functional teams, including investigators, vendors, and regulatory bodies.
- Monitor trial progress and manage data collection to ensure accuracy and integrity.
- Identify and mitigate project risks
- Oversee a team of regional CPMs, CRAs and CTAs.
- Ensure the preparation and submission of regulatory documents are compliant with local regulatory standards and maintained per good clinical practice.
- Conduct regular meetings with study teams and provide updates to stakeholders.
- Coordinate with external vendors and partners involved in the trial
- Support development of key process initiatives and SOPs internally
- Oversee vendors supporting trial execution
Benefits
- 100% paid employee premiums for medical/dental/vision
- STD
- LTD
- a 401(k) plan with a 50% company match of up to 3%
- vesting schedule of only 5 years
- 15 PTO days per year
- sick leave
- 11 paid holidays
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Manager
