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Veeva Jobs in Bothell, WA (NOW HIRING)

SystImmune, Inc

Clinical Data Manager

Redmond, WA · On-site

$100K - $170K/yr

Experience working within a Clinical EDC system (e.g., Medidata Rave, Veeva EDC). * SAS programming experience. * Experience with managing Lab Data, such as PK, PD, and Biomarkers. * Detail-oriented ...

SystImmune, Inc

Clinical Data Associate

Redmond, WA · On-site

$75K - $95K/yr

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 ...

Systimmune

Clinical Data Manager

Redmond, WA · On-site

$100K - $170K/yr

Experience working within a Clinical EDC system (e.g., Medidata Rave, Veeva EDC). * SAS programming experience. * Experience with managing Lab Data, such as PK, PD, and Biomarkers. * Detail-oriented ...

Systimmune

Clinical Data Associate

Redmond, WA · On-site

$75K - $95K/yr

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 ...

Systimmune

EDC Programmer

Redmond, WA · On-site

$100K - $150K/yr

Manage integrations with third-party RTSM/IRT systems (e.g., 4G Clinical, Suvoda, YPrime, Veeva Vault RTSM), including specification development, interface testing, and ongoing operational support.

SystImmune, Inc

EDC Programmer

Redmond, WA · On-site

$100K - $150K/yr

Manage integrations with third-party RTSM/IRT systems (e.g., 4G Clinical, Suvoda, YPrime, Veeva Vault RTSM), including specification development, interface testing, and ongoing operational support.

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Veeva information

What skills are needed for Veeva careers?

Veeva careers typically require strong technical skills such as proficiency in cloud-based software, data management, and understanding of life sciences or healthcare industries. Additionally, skills in project management, communication, and familiarity with tools like Veeva Vault or CRM platforms are valuable for many roles.

What does Veeva do?

Veeva is a company that provides cloud-based software solutions for the life sciences industry, including tools for customer relationship management, content management, and data management. Jobs at Veeva often require knowledge of software development, data analysis, or industry-specific regulations. Employees typically work in a technology-driven environment with a focus on compliance and innovation.

What is a Veeva job?

A Veeva job typically refers to a role involving Veeva Systems' software, which is used primarily in the life sciences industry for CRM, content management, and regulatory compliance. Professionals in Veeva roles may work as administrators, developers, consultants, or business analysts, focusing on implementing, configuring, or managing Veeva applications like Veeva Vault or Veeva CRM. These roles often require expertise in cloud-based software, data management, and industry-specific regulations.

What are the key skills and qualifications needed to thrive in the Veeva position, and why are they important?

To thrive in a Veeva Specialist or Consultant role, you need a strong understanding of Veeva Vault or Veeva CRM platforms, combined with expertise in life sciences business processes and data management. Familiarity with software configuration, data migration, and certifications like Veeva Vault Administrator or Veeva CRM certification are often required. Excellent problem-solving abilities, communication skills, and the capacity to collaborate effectively with cross-functional teams distinguish top performers in this position. These competencies are critical for supporting efficient system implementations, ensuring compliance, and driving user adoption in regulated industries.

What are some typical responsibilities of a Veeva Specialist or Consultant on a day-to-day basis?

As a Veeva Specialist or Consultant, your daily responsibilities may include configuring Veeva Vault or Veeva CRM systems, managing user access, supporting system integrations, and responding to end-user support requests. You'll work closely with business stakeholders to gather requirements, troubleshoot issues, and ensure the software aligns with regulatory requirements in the life sciences sector. Additionally, you might collaborate with project managers, IT, and compliance teams to support new releases or process improvements. This role often requires balancing technical tasks with user training and ongoing documentation.

Is Veeva good to work for?

Veeva is a technology company known for its cloud-based software solutions for the life sciences industry. Employees often cite a collaborative work environment, opportunities for professional growth, and a focus on innovation, though experiences can vary by role and location.

How much do Veeva Systems pay?

Veeva Systems offers salaries that vary based on role, experience, and location, with typical annual pay ranging from $70,000 to over $130,000 for software roles. Entry-level positions and roles requiring specialized skills such as cloud-based software and CRM tools tend to be on the lower to mid-range, while senior positions offer higher compensation.
What are popular job titles related to Veeva jobs in Bothell, WA? For Veeva jobs in Bothell, WA, the most frequently searched job titles are:
What job categories do people searching Veeva jobs in Bothell, WA look for? The top searched job categories for Veeva jobs in Bothell, WA are:
What cities near Bothell, WA are hiring for Veeva jobs? Cities near Bothell, WA with the most Veeva job openings:
Veeva jobs near you
Infographic showing various Veeva job openings in Bothell, WA as of June 2026, with employment types broken down into 85% Full Time, 8% Part Time, 1% Temporary, and 6% Contract. Highlights an 76% Physical, 7% Hybrid, and 17% Remote job distribution.
Clinical Data Manager

Clinical Data Manager

SystImmune, Inc

Redmond, WA • On-site

$100K - $170K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 17 days ago

Job description

SystImmune Inc. is a clinical-stage biopharmaceutical company located in Redmond, WA. 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 several assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials, SystImmune has a strong preclinical pipeline of potential cancer therapeutics in the discovery or IND-enabling stages, representing cutting-edge biologics development.
The Clinical Data Manager (CDM) plays a broad role in interfacing with clinical study teams, external partners, and vendors to design, configure, and test clinical database systems, conduct data review, and support company deliverables. The CDM will support and/or lead clinical database design, data collection and validation, data management, and reporting work for clinical trials. Additionally, the CDM will play a key role in overseeing CROs and vendors to meet study needs and deliverables.
This position requires you to be onsite full-time in Redmond, WA.Responsibilities:
  • Leads all DM lifecycle activities, from study start-up, maintenance, database lock and close-out.
  • Independently develop DM documents including but not limited to Data Management Plans (DMP), Case Report Forms (CRFs), CRF Completion Guidelines, Edit Checks, UAT specifications, centralized monitoring plans, data flow and integrity plans, blinding plans, and data review plans. Utilize templates and standard guidelines to initiate documents, but demonstrate critical thinking, alignment-building and discretion to tailor documents to study needs.
  • Independently lead data cleaning activities such as, but not limited to, study team data reviews, Non-system Edit Check Output review, SAE reconciliation, and non-CRF data reconciliation. Gather cross-functional input to drive creation of custom data review plans. Evaluate options and exercise discretion to choose efficient and effective issues resolution paths.
  • Manage data deliverables processes and database locks, with high quality and efficiency.
  • Foster collaboration and relationship-building with all study team representatives (e.g. Biostatisticians, Statistical Programmers, Medical Monitors, Clinical Scientists, Clinical Project Managers, Clinical Trial Managers, CRAs, Clinical Pharmacologists, Biomarker/Bioinformatics Scientists, Medical Writers, Regulatory representatives, etc.)
  • DM Project Management: With oversight, ensure data management deliverables are met on time. Utilize communication, available metrics reports, experience, knowledge, and other resources to efficiently lead and coordinate all data management activities. Ensure study team members from different functional areas understand and deliver components affecting data to ensure successful execution of deliverables. Provide solutions for data management issues that arise during study conduct.
  • Manage/coordinate work performed by vendors/CROs as appropriate to ensure quality of product. Assist in the selection of vendors/CROs (e.g. review RFPs, attend site audits)
  • Performs Medical Coding as needed, works with CROs, Medical Monitors, and Clinical Scientists to coordinate activities for the medical review of clinical trial data.
  • Run SAS and/or R programs, review SAS and/or R logs, troubleshoot errors, and generate output. Program SAS and/or R Non-System Edit Checks/Back-end checks and SAS and/or R Data Listings as appropriate for skill level.
  • Evaluate CDM processes and applications for improvements; participate in working groups to develop and implement new processes and applications.
  • Participate in development of DM specific SOPs.
  • Responsible for oversight of CRO data management activities and integrating the various functional group input.
  • All other duties as assigned.
Qualifications:
  • BA or BS and a minimum of 4 years of relevant experience.
  • Technologically savvy; quickly picks-up new information, standards, regulations, tools, methods or software as it relates to position and profession.
  • Experience working within a Clinical EDC system (e.g., Medidata Rave, Veeva EDC).
  • SAS programming experience.
  • Experience with managing Lab Data, such as PK, PD, and Biomarkers.
  • Detail-oriented; performs quality and accurate work.
  • Knowledgeable in GCP standards, CDISC standards (CDASH, SDTM, ADaM), FDA and ICH guidelines, and GCDMP.
  • Strong knowledge of clinical research, drug development process, and medical terminology, oncology experience preferred.
  • Knowledge and understanding of DM Lifecycle associated with P1-P3 studies, including pivotal, blinded, and randomized trials.
  • Knowledge of MedDRA and WHO Drug coding.
  • Project Management skills, ability to manage multiple projects and meet deadlines.
  • Strong interpersonal, organizational, and communication skills.
  • Prior experience writing specification documents and/or work instructions.
  • Previous vendor/CRO management.
  • Previous experience with RTSM, eCOA/ePRO systems.

Compensation and Benefits:
The expected base salary range for this position is $100,000 - $170,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate's 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 align strongly with 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.

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