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DevOps Test Engineer for EDC

Remote: 
Hybrid
Contract: 
Experience: 
Senior (5-10 years)
Work from: 
Mexico City (MX)

Offer summary

Qualifications:

Bachelor's or Master's degree in computer science or life science., 8+ years of related IT/CRO/Pharma experience., Extensive experience with Medidata RAVE UI., Strong communication and interpersonal skills., Familiarity with clinical data standards and guidelines..

Key responsabilities:

  • Facilitate discussions with stakeholders and provide technical support.
  • Perform change impact analysis and risk assessments.
  • Follow validation lifecycle for system upgrades and changes.
  • Create GxP validation test cases and execute test plans.
  • Update incident management tools regarding ongoing tasks.
AstraZeneca logo
AstraZeneca Pharmaceuticals XLarge http://www.astrazeneca.com/
10001 Employees
See more AstraZeneca offers

Job description

AstraZeneca is currently looking for EDC Functional Test Engineer to join our R&D IT: EDC Product Team to help support, manage and maintain our EDC product along with it’s numerous integration products.  AZ’s EDC System is Medidata’s Rave, and at AZ is GxP compliant and part of Clinical Development Platforms and is used across late science teams across all therapeutic areas. You will be a part of our BizDevOps team therefore will be responsible to work cross functionally with other team members such as Product Lead, DevOps Lead and Release manager & other technical engineers.

Key Responsibilities:

  • Facilitate key discussions with various stakeholders as requested by system owner/platform lead and provide SME technical support on system testing of the Core EDC Product, and any data integrations (in and out) of EDC.
  • Perform impact analysis for any change that happens on the EDC system
  • Work with business and perform risk assessment during change implementations/ system upgrades or updates to integrations
  • Follow and participate in validation lifecycle for upgrades, changes, & new integrations
  • Co-develop validation packages in accordance with standard operating procedures (SOPs).
  • Provide support of code review and solutioning for downstream customer requirements, including data extraction methods (SQL, Webservices, APIs)
  • Actively participate in business meetings and bring new ideas to the table
  • Responsible to solve day-to-day incidents, service requests and work towards incident-reduction and automation. Also, update Service Now (ticket management tool) for all events with respect to the incidents, service requests, changes and problems.
  • Constantly thrive to learn and upskill according to the organization’s goals and demands.
  • Create Gxp Validation Test cases in Jira Xray for system/upgrade testing
  • Perform validation test executions in Jira Xray, for both system testing and regression testing.
  • Assist in creating or create UAT test cases that cover the essential business scenarios/use cases for the business.
  • Facilitate process requirements gathering: capturing user stories, requirement analysis, data analysis, programming, database management, and systems integration.

Mandatory Skills

  • Extensive experience of using Medidata RAVE UI or any CSV Computer System Validation (Classic or Rave EDC) to perform the following actions:
    • Study build, edit checks programming, deployment to production and migration
    • Understanding about different roles and permissions in Rave
    • Understanding of core configuration and clinical views
    • Understanding of what data extraction capabilities there are
    • Hands on Experience of Inbound Rave Web Services (eg IVRS or discrepancy inputs)
    • Experience of setting up Rave safety gateway (RSG) and SAE notifications
    • Experience of setting up SAS extracts
    • Experience on setting up Target Source Data Verification (TSDV)
  • Hands on experience of being involved in URL upgrade(s) (Medidata release updates)
  • Knowledge on system validation process / Application Life Cycle Management
  • Must have strong communication skills and interpersonal skills
  • Responsible to work on technical tasks to keep the Rave URL(s) and it’s integrations in a maintained state
  • Adhere to AZ core ITIL guidelines and perform tasks as incident, change, problem etc.
  • Working experience in clinical standard and data collection, clinical data conversion or clinical data programming/testing.
  • Understanding of CDASH, SDTM, ADaM CDISC controlled Terminology and FDA/ICH guidelines for clinical study data
  • Effective in stakeholder management, translating technical concepts, and working within team environments.
  • Skilled in project management basics and creating clear technical documentation.

Preferred Skills

  • Hands on Experience of custom function, SAS  programming
  • Knowledge on Coder / Coder+ setup & Lab setup
  • Hands on Experience of outbound Rave Web Services (ODM Adapter, Biostats Adapter)
  • Hands on Experience of Rave backend data model, sql script writing, stored procedures
  • Hands-on knowledge in agile management tools like Service NOW
  • Hands-on experience in performing system testing including authoring and executing test cases
  • Passion for learning, innovating, and delivering valuable software to people.
  • Any other programming languages/technical skills e.g: Python, JAVA, etc.
  • Knowledge of other Medidata products and/or Cloud
  • EDC testing (Rave/Inform/Veeva) experience.

Educational Requirements

  • Bachelor or master’s degree in computer science or life science related discipline with IT/CRO/Pharma experience with total of 8+ years of experience

📌Strong English communication skills required.

📌 Positions are open to Mexican Citizens and official residents of Mexico.


📍 Location: Guadalajara (hybrid - Expectation of working in the office 3 days a week)
When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working give us the platform we need to connect, work at pace and challenge perceptions. That’s why we work, on average, a minimum of three days per week from the office. But that doesn’t mean we’re not flexible. We balance the expectation of being in the office while respecting individual flexibility.

Why AstraZeneca?

At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognising their potential. Join us on our journey of building a new kind of organisation to reset expectations of what a bio-pharmaceutical company can be. This means we’re opening new ways to work, pioneering cutting edge methods and bringing unexpected teams together.

Interested? Come and join our journey.

So, what’s next!

Are you already imagining yourself joining our team? Good, because we can’t wait to hear from you.

Where can I find out more?

Our Social Media:

Follow AstraZeneca on LinkedIn https://www.linkedin.com/company/1603/

Follow AstraZeneca on Facebook https://www.facebook.com/astrazenecacareers/

Follow AstraZeneca on Instagram https://www.instagram.com/astrazeneca_careers/?hl=en

AstraZeneca is an equal opportunity employer.

AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law. AstraZeneca only employs individuals with the right to work in the country/ies where the role is advertised.

Date Posted

08-nov-2024

Closing Date

19-ene-2025

AstraZeneca embraces diversity and equality of opportunity.  We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.  We believe that the more inclusive we are, the better our work will be.  We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.  We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

Required profile

Experience

Level of experience: Senior (5-10 years)
Industry :
Pharmaceuticals
Spoken language(s):
EnglishEnglish
Check out the description to know which languages are mandatory.

Other Skills

  • Social Skills
  • Verbal Communication Skills

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