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Senior Clinical Data Associate Jobs in Bothell, WA

ACES

Sr. Clinical Manager - SV Administration

Bellevue, WA

$25.75 - $33.75/hr

JOB MISSION AND SUMMARY The mission of the Senior Clinical Manager- SV Administration is to provide ... Data Collection and Leadership Support: Monitor TSR conversion, complete planner, productivity ...

ACES

Sr. Clinical Manager - SV Administration

Bellevue, WA · On-site

$102K - $110K/yr

JOB MISSION AND SUMMARY The mission of the Senior Clinical Manager- SV Administration is to provide ... Data Collection and Leadership Support: Monitor TSR conversion, complete planner, productivity ...

Pfizer

Head of AI Clinical Excellence

Bothell, WA · On-site

$89K - $121K/yr

... data review, study execution, operational efficiency, decision-making, and regulatory readiness ... Serve as a trusted advisor to senior leaders on emerging AI capabilities, industry trends, and ...

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All JobsClinical Data Associate JobsSenior Clinical Data Associate JobsSenior Clinical Data Associate Jobs in Bothell, WA

Senior Clinical Data Associate information

See Bothell, WA salary details

$44.2K

$65.9K

$82.2K

How much do senior clinical data associate jobs pay per year?

As of Aug 16, 2026, the average yearly pay for senior clinical data associate in Bothell, WA is $65,885.00, according to ZipRecruiter salary data. Most workers in this role earn between $51,400.00 and $75,500.00 per year, depending on experience, location, and employer.

What are some common challenges senior clinical data associates face when managing large clinical trial datasets?

Senior Clinical Data Associates often manage complex datasets from multiple sites, which can lead to challenges such as ensuring data consistency across sources, resolving discrepancies, and maintaining data integrity under tight timelines. Additionally, they must stay up-to-date with evolving regulatory requirements and work closely with cross-functional teams, including biostatisticians, clinical operations, and data managers, to ensure accurate and timely data delivery. Effective communication, attention to detail, and adaptability are essential to overcome these challenges and ensure successful trial outcomes.

What are the key skills and qualifications needed to thrive as a senior clinical data associate?

To thrive as a Senior Clinical Data Associate, you need expertise in clinical data management, data cleaning, and knowledge of clinical trial processes, supported by a degree in life sciences or a related field. Familiarity with data management systems like Medidata Rave, EDC platforms, and certifications such as CCDM are commonly required. Attention to detail, strong analytical thinking, and effective communication skills help you excel in ensuring data accuracy and collaborating with cross-functional teams. These capabilities are crucial for maintaining data integrity, regulatory compliance, and the overall success of clinical research studies.

What does a senior clinical data associate do?

A Senior Clinical Data Associate is responsible for managing and ensuring the accuracy, integrity, and quality of data collected during clinical trials. They oversee data collection processes, review case report forms, resolve data discrepancies, and ensure compliance with regulatory standards. In addition to performing data management tasks, Senior Clinical Data Associates often mentor junior staff, contribute to developing data management plans, and collaborate with clinical research teams to ensure successful trial outcomes.

What cities near Bothell, WA are hiring for Senior Clinical Data Associate jobs?

Cities near Bothell, WA with the most Senior Clinical Data Associate job openings:

Senior Clinical Data Associate jobs near you

Clinical Development Scientist

ComTec Information Systems

Bothell, WA • On-site

Contractor

Re-posted 7 days ago

Job description

Job Title - Clinical Development Scientist;
Hybrid role. 3 days/week in office
Bothell WA/Cambridge MA/ Plymouth MN

12 Months


Ultrasound, Senior Clinical Development Scientist The Senior Clinical Development Scientist for the Ultrasound group will be responsible for developing, generating, and disseminating clinical and economic evidence ensuring innovation, and transformation with best-in-class clinical evidence. Your role: Contribute strategic guidance for clinical and economic evidence related to the end to end (E2E) development process from ideation through post-market for products in the Ultrasound business. Collaborate with key internal and external stakeholders to provide in-depth expertise to develop and lead clinical initiatives through non-clinical and clinical strategies for new product development initiatives and product life cycle management. Drive execution ensuring quality and timeliness of clinical programs and/or trials to support critical regulatory requirements, be agile and responsive during course of design, execution, and interpretation of trial data. Collaborate with investigators, IRBs/ECs, Regulatory Agencies, societies, and associations; and additionally, to support claims, reimbursement, health economic outcomes and/or market access. Ensure appropriate preparation, interpretation and dissemination of all evidence generated, including Clinical Study Reports (CSRs), Clinical Evaluation Reports (CERs), abstracts, peer-reviewed manuscripts, as assigned. Lead or support scientific discussions with regulatory agencies or notified bodies, including proposed clinical investigations; review process of clinical evidence generated for marketing authorization, in line extensions, including during sponsor regulatory inspections.

You are the right fit if:

You have acquired 7+ years of experience in clinical research/development/real world evidence (RWE); scientific study design, strong scientific background and experience with Artificial Intelligence algorithm clinical performance validation. You have deep expertise including innovative clinical trial design, registries, quality improvement initiatives, and creation of data networks and working knowledge of biostatistics. Your skills include a demonstrated working knowledge of GCP, FDA regulations and EU-MDR regulations, and in-depth understanding of product development and associated design controls for medical devices. You have strong writing skills to product quality clinical documents, including final reports. Strong knowledge and experience with study design is also desired. You have an ability to write original scientific documentation such as clinical study reports, regulatory filings, investigator brochures, clinical evaluation reports, internal reports and scientific publications. You have a medical or scientific education (MD or PhD). You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this Clinical position. You are self-directed with a strong work ethic, agile, and have an ability to work in a purposeful environment. You can collaborate effectively and influence decision making with various teams cross-functionally, as well as externally. You can think analytically, present statistical methods and results to a variety of audiences, especially non-statisticians. You can travel up to 15% (domestic and international) according to business needs.,