SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials, SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discovery or IND-enabling stages, representing cutting-edge biologics development.
We are seeking a highly skilled and motivated Senior Global Director, Clinical Project Management (CPM) to join our 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 Senior Global Director, Clinical Project Management, will play a critical role in delivering high-quality data and ensuring the success of clinical studies.
Key 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
Qualifications
Bachelor’s degree in Life Sciences, Nursing, or a related field.
Minimum of 15 years of experience in Clinical Trial Management, including demonstrated people leadership and direct line management experience.
Strong experience working on early phase studies required, late phase studies experience is a plus.
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
Location/Travel:
Princeton NJ hybrid, 3 days in office
Overnight travel ~25%
The expected base salary range for this position is $220,000 - $280,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate’s qualifications, experience, and skills.
SystImmune is a leading and well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company’s success. SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE.
We offer an opportunity for you to learn and grow while making significant contributions to the company’s success.
SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.
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Numbers & Facts
Location
Princeton, NJ
Job Type
Full-time
Website
https://systimmune.com/
Skills
Antibodiesunmatched
Biologyunmatched
Biotech and Pharmaceuticalunmatched
Budgetingunmatched
Cancerunmatched
Clinical Trialunmatched
Clinical Trial Managementunmatched
Communication Skillsunmatched
Cross-Functionalunmatched
Data Collectionunmatched
Data Managementunmatched
Data Qualityunmatched
Drug Developmentunmatched
GCP (Good Clinical Practices)unmatched
Hematologyunmatched
Interpersonal Skillsunmatched
Leadershipunmatched
Maintain Complianceunmatched
Multitaskingunmatched
Nursingunmatched
Oncologyunmatched
Organizational Skillsunmatched
Project/Program Managementunmatched
Regulationsunmatched
Regulatory Complianceunmatched
Regulatory Requirementsunmatched
Regulatory Submissionsunmatched
Research Protocolsunmatched
Risk Managementunmatched
Standard Operating Procedures (SOP)unmatched
Team Lead/Managerunmatched
Team Playerunmatched
Time Managementunmatched
Vendor/Supplier Evaluationunmatched
Willing to Travelunmatched
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