Clinical Data Associate

Syst Immune is a leading, well‑funded clinical‑stage biopharmaceutical company located in Redmond, WA and Princeton, NJ, specializing in innovative cancer treatments using bi‑specific, multi‑specific antibodies, and antibody‑drug conjugates (ADCs). The company has multiple assets in various stages of clinical trials for solid tumor and hematologic indications, along with a robust preclinical pipeline.

Clinical Data Associate (CDA)

This role is full‑time onsite in Redmond, WA. The company will relocate to a new facility in Bothell, WA in the fall.

• Support the CDM in day‑to‑day data management activities across study start‑up, maintenance, and close‑out, including tracking open queries and data cleaning timelines.
• Assist in the development and review of DM documents such as Data Management Plans, CRF Completion Guidelines, and data review plans using established templates and standards.
• Perform data review activities including query generation, query resolution follow‑up, and non‑system edit check output review under CDM oversight.
• Assist with SAE reconciliation and non‑CRF data reconciliation activities, escalating issues to the CDM as appropriate.
• Support medical coding activities using MedDRA and WHO Drug dictionaries, coordinating with the CDM and CRO for medical review.
• Run and review SAS and/or R programs and data listings as directed; assist in troubleshooting basic programming errors under CDM guidance.
• Perform UAT of EDC systems and edit checks per provided specifications and test scripts.
• Assist in tracking and coordinating CRO/vendor deliverables, flagging risks or delays to the CDM.
• Contribute to data quality monitoring by reviewing metrics reports and flagging trends or anomalies to the CDM.
• Support database lock activities by assisting with lock checklists, outstanding query resolution, and coordination tasks.
• Participate in the development and review of DM SOPs and process improvement initiatives.
• All other duties as assigned.

• BA or BS in life sciences, health informatics, or a related field.
• 1–3 years of relevant clinical data management or clinical research experience; equivalent internship or co‑op experience in a clinical or pharma setting will be considered.
• Exposure to a Clinical EDC system (e.g., Medidata Rave, Veeva EDC) preferred.
• SAS, Python, and R programming knowledge is a plus.
• Familiarity with CDISC standards (CDASH, SDTM) and GCP guidelines preferred; willingness to develop deep knowledge required.
• Detail‑oriented with strong organizational and time‑management skills.
• Effective written and verbal communication skills; ability to work cross‑functionally.
• Eagerness to learn in a fast‑paced, clinical‑stage biopharmaceutical environment.
• Oncology experience or interest a plus.

The expected base salary range for this position is $75,000 – $95,000 annually, with actual compensation based on a variety of factors, including level of qualifications, experience, and skills. Most offers typically fall within the low to mid‑point of the range, with potential for higher compensation for exceptional candidates.

Benefits include: 100% paid employee premiums for medical/dental/vision, STD, LTD, a 401(k) plan with a 50% company match up to 3%, vesting schedule of 5 years, 15 PTO days per year, sick leave, 11 paid holidays, and additional benefits.

Syst Immune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.