Associate Director of Project Management Visa Sponsorship Jobs in New Jersey
Associate director of project management visa sponsorship jobs in New Jersey are concentrated in pharma and life sciences corridors around Parsippany, Bridgewater, and Princeton, with major employers including Johnson & Johnson, Merck, and Cognizant. Financial services and tech firms in Jersey City and Newark also sponsor for senior PM leadership roles regularly.
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SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Bothell, 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 and IND-enabling stages, representing cutting-edge biologics development. We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
We are seeking a highly skilled and motivated Associate 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 Associate 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.
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 7 years of experience in clinical trial management with a preference of leading Clinical Operations team (CRA, SSU, CTM)
- Experience in managing global oncology trials
- 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
- 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
LOCATION/TRAVEL:
- Princeton NJ onsite in office
- Overnight travel ~25%
COMPENSATION AND BENEFITS:
The expected base salary range for this position is $150,000- $180,000 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.
INTRODUCTION
SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Bothell, 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 and IND-enabling stages, representing cutting-edge biologics development. We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
We are seeking a highly skilled and motivated Associate 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 Associate 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.
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 7 years of experience in clinical trial management with a preference of leading Clinical Operations team (CRA, SSU, CTM)
- Experience in managing global oncology trials
- 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
- 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
LOCATION/TRAVEL:
- Princeton NJ onsite in office
- Overnight travel ~25%
COMPENSATION AND BENEFITS:
The expected base salary range for this position is $150,000- $180,000 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.
Associate Director of Project Management Job Roles in New Jersey
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Search Associate Director of Project Management Jobs in New JerseyAssociate Director of Project Management Jobs in New Jersey: Frequently Asked Questions
Which companies sponsor visas for associate directors of project management in New Jersey?
Pharmaceutical and life sciences employers are among the most active sponsors for this role in New Jersey, including Johnson & Johnson, Merck, Novartis, and Becton Dickinson. Large IT services and consulting firms such as Cognizant, Infosys, and Tata Consultancy Services also file sponsorship petitions regularly for senior project management leadership positions across the state.
What visa types realistically apply to associate director of project management roles in New Jersey?
The H-1B visa is the most common path, as the role qualifies as a specialty occupation requiring a directly related bachelor's degree or higher. Australian nationals can pursue the E-3 visa, and Chilean or Singaporean nationals may qualify under the H-1B1 visa. Those already holding H-1B visa status with a new employer filing a petition can start the new role once that petition is filed. EB-2 and EB-3 green card sponsorship is also available through PERM labor certification for longer-term placements.
Which cities in New Jersey have the most associate director of project management sponsorship jobs?
Parsippany and Bridgewater are leading hubs due to the dense concentration of pharmaceutical headquarters. Princeton draws sponsors in both biotech and financial technology. Jersey City and Newark attract financial services and professional services firms with active sponsorship histories. The I-287 corridor broadly connects many of New Jersey's largest corporate campuses where senior PM roles are regularly filled through visa sponsorship.
How to find associate director of project management visa sponsorship jobs in New Jersey?
Migrate Mate is the most direct way to search, as the platform lists New Jersey employers with verified sponsorship histories specifically for project management leadership roles. Filtering by role and location surfaces companies that have actively filed for comparable positions, so you can focus your applications on employers with a demonstrated track record rather than applying broadly and asking about sponsorship later in the process.
Are there any New Jersey-specific considerations for associate directors of project management seeking visa sponsorship?
New Jersey's pharma and life sciences sector creates consistent demand for senior project managers who can oversee cross-functional clinical, regulatory, and product development programs, making the degree-to-role match for specialty occupation requirements relatively straightforward. Employers in this sector often have established immigration counsel and structured sponsorship programs. F-1 students on OPT from Rutgers, Stevens Institute of Technology, or New Jersey Institute of Technology sometimes transition into associate director tracks at local employers after several years of progression.
What is the prevailing wage for sponsored associate director of project management jobs in New Jersey?
U.S. employers sponsoring a visa must pay at least the prevailing wage, which is what workers in the same role, area, and experience level typically earn. The Department of Labor sets this rate to make sure companies aren't hiring foreign workers simply because they'd accept lower pay than a U.S. worker. It varies by job title, location, and experience. You can look up current prevailing wage rates for any occupation and location using the OFLC Wage Search page.