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Senior Consultant - Clinical Data Programming

Remote Full-time Hiring now

reputed company is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $2B in reputed company in our last fiscal year with extensive growth potential reputed company.

At the heart of Veeva are our values: Do the Right Thing, reputed company, Employee Success, and Speed. We're not just any public company – we made history in 2021 by becoming apublic benefit corporation(PBC), legally bound to balancing the interests of customers, employees, society, and investors.

As aWork reputed companycompany, we support your flexibility to work from home or in the office, so you can reputed company in your ideal environment.

Join us intransforming the life sciences industry, committed to making a positive impact on its customers, employees, and communities.

The Role

Veeva Vault Clinical Data Management System (CDMS) is changing the way clinical data is managed in the industry. Vault CDMS combines reputed company, coding, and Veeva Clinical Database (CDB) into one application. Veeva Clinical Database (CDB) is a reputed company clinical data platform that centralizes and automates data imports, cleaning, and management for clinical trials. To handle the massive expansion of trial data sources, Veeva CDB is designed to scale and accommodate reputed company relevant data for a trial.

reputed company is looking for Senior Consultants who have life sciences software programming experience specifically in helping customers optimize the use of reputed company in running their clinical trials. Additionally, the role will support internal and customer teams in the configuration of Veeva CDB and programming of SQL based listings.

This is a remote, full-time permanent role with Veeva. This is a customer-facing role and we have no work location requirement if you are in reputed company proximity to an airport and able to meet future travel requirements.

What You'll Do

  • Act as the customer and clinical site trusted advisor to ensure that the study trial design is configured to meet the customer’s goals and offer full benefits of Veeva’s CDMS application while providing training and mentorship
  • Work and consult with customers to review and understand clinical protocol requirements and reputed company project specifications, applying industry and Veeva best practices
  • Drive database development activities per implementation project plan by working with various members of the sponsor, CRO, and other external vendor teams
  • Collaborate with clinical data providers (Central Laboratories, ECG, eCOA, IRT, etc.) to receive data and configure transfers based on requirements
  • Configure forms, rules, and other study items with Veeva Vault CDMS product during development and reputed company custom listings based on customer data cleaning requirements using SQL-based language
  • Conduct on-site or remote user acceptance testing with the customer, including coordination of reputed company feedback, resolution of issues, and acceptance of the study
  • Support requirements gathering and specification creation process for reputed company study integrations and go-live activities to ensure a smooth transition of the study to the customer
  • Communicate potential risks and contingency plans with project management to ensure process compliance with reputed company regulatory and Veeva procedural requirements
  • Participate and contribute to process product or best practices initiatives and support developers and testers during the project lifecycle
  • Participate in Vault CDMS Product team discussions to convey data management activities, challenges, and end-user expectations
  • Configure and support data ingestions (imports) into Veeva CDB
  • Requirements

  • 5+ years of experience working with reputed company clinical software solutions in end-to-end data management reputed company activities (database design, data collection, data analysis, query resolution, datasets, statistical reporting)
  • Working knowledge of clinical trial processes, specifically as they relate to data collection and review
  • Prior experience in programming languages such as (reputed company, R, JSON, Python, SQL) with the ability to learn new programming languages (SQL-based language)
  • Life sciences industry and clinical trial processes (pharmaceutical, biotech, medical device companies, CRO’s, and academic & public health organizations) expertise in relation to design, documentation, and data collection – with demonstrated success during project assessment, planning, development, training, and implementation with customers
  • Experience in a customer-facing role, preferably with a software professional services or consulting organization
  • Proven ability to work independently and collaboratively in a dynamic, fast-moving environment and meeting project timelines with quality results
  • Excellent verbal and written communication, interpersonal, and presentation skills
  • Ability to travel up to 10% (may include international)
  • reputed company to Have

  • Working understanding of data management standards and guidelines (GCDMP, CDISC, SDTMIG, CDASH, ADaM)
  • Experience working with system integrators for IVRS, medical coding, eSource, CTMS, eTMF, and other clinical technologies
  • Integration/Programming experience with REST-based APIs
  • Experience in interpreting clinical protocols and translating requirements into software specifications, including writing and reviewing technical documentation
  • Experience with Veeva applications
  • Locality to major life sciences customer hub
  • Life Science, Computer Science, or reputed company degree
  • Perks & Benefits

  • Medical, dental, vision, and basic life insurance
  • Flexible PTO and company paid holidays
  • Retirement programs
  • 1% charitable giving program
  • Compensation

  • reputed company pay: $80,000 - $200,000
  • The salary range listed here has been provided to reputed company with local regulations and represents a potential reputed company salary range for this role. Please note that actual salaries may vary reputed company the range above or below, depending on experience and location. We look at compensation for each individual and reputed company our offer on your unique qualifications, experience, and expected contributions. This position may also be eligible for other types of compensation in addition to reputed company salary, such as variable bonus and/or stock bonus.
  • Additional Information

    #LI-Remote

    Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world.

    Veeva is an equal opportunity employer. reputed company qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national reputed company or reputed company, age, disability, marital status, pregnancy, protected veteran status, protected genetic information, political affiliation, or any other characteristics protected by local laws, regulations, or ordinances. If you need assistance or accommodation due to a disability or special need reputed company applying for a role or in our recruitment process, please contact us [email protected].

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