Clinical Scientist - Oncology

SystImmune; Princeton (NJ); On-site; USD 80,000 - 130,000; Full time

Benefits offered by this job

Health/dental/vision fully paid

STD/LTD

401(k) matching

PTO 15 days

Holidays 11

Vesting 5 years

Job summary

SystImmune, Inc. is seeking a Clinical Scientist to join our clinical development team in Princeton, NJ. The role offers hands-on experience in trial design, data analysis, and regulatory documentation within a fast-moving biotech environment.

You will monitor safety and efficacy data, translate protocols into deliverables, and collaborate closely with clinicians, statisticians, and data managers to advance our oncology programs. Competitive salary and comprehensive benefits provided.

Qualifications

• Degree in life sciences or health-related field.
• Minimum 3–4 years industry experience, clinical research preferred.
• Oncology therapeutic area expertise required.
• Experience with data cleaning, visualization, and basic statistical analysis (Excel mandatory, R optional).
• Knowledge of ICH, GCP, and regulatory guidelines.
• Ability to analyze and socialize data to stakeholders.
• Strong communication, presentation, and teamwork skills.
• Ability to think strategically and work independently to meet timelines.

Responsibilities

• Monitor, review, and summarize safety and efficacy data in ongoing studies.
• Collaborate with clinical team to translate protocol into deliverables and study plans.
• Respond to study questions from sites/vendors with supervision.
• Perform literature searches and review to support trial design and regulatory documents.
• Support preparation of scientific material.
• Develop SOPs and guidelines and templates.
• Participate in cross-functional team meetings with clinical operations, safety, regulatory, biostatistics and data management.

Skills

Data analysis

Data visualization

Statistical analysis

Excel

ICH/GCP knowledge

Communication

Collaboration

Strategic thinking

Independent work

Education

Bachelor's degree in life sciences

Tools

Excel

R

Job description

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 discover 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 motivated Clinical Scientist to join our clinical development team and contribute to the advancement of innovative therapeutic programs. This role provides an excellent opportunity to gain hands-on experience in clinical trial design and execution while working alongside experienced clinical development professionals in a dynamic biotech/pharmaceutical environment.

Responsibilities

• Monitor, review, and summarize safety and efficacy data in 1 or more ongoing studies on a regular basis
• Work in close collaboration with the clinical team to ensure translation of the clinical protocol (and amendments) into operational deliverables, including but not limited to performing ongoing review and analysis of clinical study data and preparing/reviewing study plans (i.e., Medical Monitoring, Medical Data Review, Safety Management, CRF Completion Guidelines, etc.)
• Respond to study questions from sites and/or vendors, with study medical monitor or Clinical Development supervision where needed
• Perform literature search and critically review and summarize the relevant scientific, drug development, and medical literature to support new clinical trial design as well as the development of clinical and/or regulatory documents
• Support preparation of scientific material
• Contribute to the development of SOPs and associated guidelines and templates
• Participate in cross-functional team meetings with members from clinical operations, safety, regulatory, biostatistics and data management

Qualifications

• Degree in life sciences or health-related field
• Minimum requirement: at least 3-4 years’ industry experience (clinical research preferred)
• Therapeutic areas of expertise must include oncology
• Experience with data cleaning, visualization, and basic statistical analysis (Excel mandatory, R optional)
• Knowledge of the International Council of Harmonization (ICH), GCP, and other relevant regulatory guidelines
• Ability to analyze, interpret and socialize data to internal and external stakeholders
• Strong communication, presentation, analytic, and strategic capabilities and ability to effectively collaborate with medical experts
• Ability to think strategically and creatively, function independently, deliver on timelines, and contribute strategic insights

Compensation and Benefits:

The expected base salary range for this position is $80,000 to $130,000 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.