Top 13 Clinical data associate Jobs in Everett Wa

Clinical Data Associate
SystImmune —Redmond, WA
- $75,000 - $95,000 a year
- Full-time
- Bachelor of Science
- Bachelor's degree
- Continuous improvement
- Paid holidays
- Disability insurance
Clinical Research Coordinator I
Fred Hutchinson Cancer Center —Seattle, WA
- $27.01 - $38.45 an hour
- Full-time
- Bachelor of Science
- High school diploma or GED
- Bachelor's degree
- Paid parental leave
- Paid holidays
Administrative Assistant - Regulatory
Eastside Research Associates —Redmond, WA
- $24 - $26 an hour
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Office
- Health savings account
- Health insurance
1d
Regulatory Coordinator I/II - Lab Based Studies
Fred Hutchinson Cancer Center —Seattle, WA
- $28.36 - $50.12 an hour
- Full-time
- Hybrid work
- Mid-level
- High school diploma or GED
- Associate's degree
- Paid parental leave
- Paid holidays
Clinical Research Coordinator II
Fred Hutchinson Cancer Center —Seattle, WA
- $31.83 - $47.73 an hour
- Full-time
- Mid-level
- High school diploma or GED
- Data entry
- Paid parental leave
- Paid holidays
7d
Regulatory and Data Coordinator I
Eastside Research Associates —Redmond, WA
- $25 - $28 an hour
- Full-time
- Hybrid work
- Microsoft Excel
- Microsoft Outlook
- Bachelor's degree
- Health savings account
- Health insurance
6d
Administrative Assistant - Regulatory
ERA Health Research —Redmond, WA
- $24 - $26 an hour
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Office
- Health savings account
- Health insurance
Quick Apply
2d
Regulatory Coordinator II
Fred Hutchinson Cancer Center —Seattle, WA
- $80,172 - $104,250 a year
- Full-time
- Mid-level
- High school diploma or GED
- SharePoint
- Paid parental leave
- Paid holidays
19h
Trial Master File Lead - TMF
Sound Pharmaceuticals Inc —Seattle, WA
- $80,000 - $120,000 a year
- Email
- Hybrid work
- Microsoft Outlook
- 5 years
- Databases
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Coordinator On Site - Okinawa, Japan
Arcetyp LLC —Seattle, WA
- Full-time
- Writing skills
- Mid-level
- Windows
Quick Apply

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Research Coordinator I
EvergreenHealth —Kirkland, WA
Extracts technical, medical and/or behavioral information from institutions or clinical records to complete case report forms. May perform phlebotomy if needed.
$31.79 - $50.85 an hour
Quick Apply
Clinical Research Coordinator I
Fred Hutchinson Cancer Center —Seattle, WA
BA/BS in a life sciences field of study. Primary responsibilities of the CRC will include assistance with the planning, coordination, implementation, and close-…
$27.01 - $38.45 an hour

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Clinical Research Coordinator
OhioHealth —Columbus, OH
This position performs basic day to day activities related to clinical research studies including recruit and screen participants, obtains informed consent,…
Clinical Research Coordinator I
Nationwide Children's Hospital —Columbus, OH
Recruits, consents and enrolls subjects according to ICH/GCP regulations, and subjects’ rights through institutional IRB, federal and state regulations; answers…

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Clinical Data Associate

SystImmune -
Redmond, WA

Apply Now

Job Details

Full-time
$75,000 - $95,000 a year

Benefits

Paid holidays
Disability insurance
Health insurance
Dental insurance
Paid time off
Vision insurance
401(k) matching

Qualifications

Data integrity assurance
Document review (document control)
Clinical research
System troubleshooting
Data validation techniques
Procedural guides
SAS
Bachelor of Science
R
Medical coding guidelines
SAS language
Bachelor's degree
Continuous improvement
System validation
Data quality monitoring
CDISC standards
User acceptance testing
Vendor communication
Clinical trial standard operating procedures
Red flag analysis
Oncology
Cross-functional collaboration
Standard operating procedures (SOPs)
Communication skills
Python
Entry level
Cross-functional communication
Statistical analysis tools
Time management

Full Job Description

Redmond, WA

Full Time

Data Management

Entry Level

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.

The Clinical Data Associate (CDA) supports the Clinical Data Manager in executing data management activities across clinical trials, with a primary focus on Phase 3 and other large-scale studies. The CDA will gain hands-on experience across the full DM lifecycle while working under the guidance of senior data management staff.

This role is full-time onsite in Redmond, WA. Please note that SystImmune plans to relocate to a new facility in Bothell, WA in the fall.

Responsibilities:

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 (User Acceptance Testing) 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.

Qualifications:

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.

Compensation and Benefits:
The expected base salary range for this position is $75,000 - $95,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate’s level qualifications, experience, and skills.
While most offers typically fall within the low to mid-point of the range, we may extend an offer toward the higher end for exceptional candidates whose background and expertise exceeds the requirements of the role.

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.

Apply Now

Refine Your Search

clinical data associate jobs in everett wa

Clinical Data Associate

Clinical Research Coordinator I

Administrative Assistant - Regulatory

Regulatory Coordinator I/II - Lab Based Studies

Clinical Research Coordinator II

Regulatory and Data Coordinator I

Administrative Assistant - Regulatory

Regulatory Coordinator II

Trial Master File Lead - TMF

Clinical Research Coordinator On Site - Okinawa, Japan

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