Senior Director, Global Clinical Project Management - Oncology

About this role

Thanks for visiting our Career Page. Please review our open positions and apply to the positions that match your qualifications.Senior Director, Global Clinical Project Management - OncologyPrinceton, NJFull TimeSenior Manager/SupervisorShareSystImmune 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 ResponsibilitiesOversee the planning and execution of global clinical trialsDevelop 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 risksOversee 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 trialSupport development of key process initiatives and SOPs internallyOversee vendors supporting trial executionQualificationsBachelor’s degree in Life Sciences, Nursing, or a related field.Minimum of15 years of experience in Clinical Trial Management, includingdemonstrated people leadership and direct line management experience.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 environmentFlexibility and adaptability to changing priorities and workloadMaster’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 hybrid, 3 days in officeOvernight travel ~25%The expected base salary range for this position is $210,000 - $260,000 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.ShareApplyApply for this positionRequired*First Name*Last Name*Email Address*Phone*AddressResume*We've received your resume.

Clickhereto update it.Attach resumeorPaste resumeAttach resume as .pdf, .doc, .docx, .odt, .txt, or .rtf (limit 5MB) orPaste resumePaste your resume here orAttach resume fileLinkedIn Profile URL:Desired salary*In 3–4 sentences, describe one global Phase III trial you directly led as the CPM.Include:• Indication (oncology or rare/complex disease)• Number of countries and regions• Your personal responsibility (what you owned, not your team)If you haven’t led a global Phase III trial, what phase have you led?*In 3–4 sentences, describe your highest-level clinical project management role.Include:• Size and location of teams you led• Global scope of the trials• Clinical systems you personally used or owned (CTMS, eTMF, EDC, etc.)*To continue, type the following sentence exactly as written, and also include the last word of the third bullet under Responsibilities in this job posting:“I confirm my application responses and are my own work and not generated by any AI tool.”Then write the extracted word from the third bullet point in box below.*The following questions are entirely optional.To comply with government Equal Employment Opportunity and/or Affirmative Action reporting regulations, we are requesting (but NOT requiring) that you enter this personal data. This information will not be used in connection with any employment decisions, and will be used solely as permitted by state and federal law. Your voluntary cooperation would be appreciated.Learn more.GenderDecline to answerFemaleMaleRace/EthnicityDecline to answerHispanic or LatinoWhite, not Hispanic or LatinoBlack or African-American, not Hispanic or LatinoAsian, not Hispanic or LatinoNative Hawaiian or Other Pacific Islander, not Hispanic or LatinoAmerican Indian or Alaskan Native, not Hispanic or LatinoTwo or More Races, not Hispanic or LatinoMENA (Middle Eastern and North African)Human Check*Submit Application