Programmer Analyst I (Clinical data managers / database designers)

Posted Yesterday
Be an Early Applicant
Hiring Remotely in Bangalore, Bengaluru Urban, Karnataka, IND
In-Office or Remote
Mid level
Biotech
The Role
The role involves programming using Medidata Rave or Veeva, managing clinical data, and developing analytics dashboards while requiring protocol interpretation skills.
Summary Generated by Built In

Job Overview:

Calling Clinical Data Managers / Database designers with strong experience in protocol interpretaion and edit checks specification keen to be trained in programming!

    Performs programming activities (using Medidata Rave or Veeva) on multiple projects concurrently with less or no support from Senior Programmers. Has strong protocol interpretation skills and understanding of Data management documents like Edit check specifications. Development and implementation of solutions to global technical service issues and concerns regarding EDC tools like Medidata RAVE or VEEVA.

      Summary of Responsibilities:

      • Performs independent programming activities on multiple projects concurrently with less or no support from Senior Programmers. Development and implementation of solutions to global technical service issues and concerns regarding EDC tools like Medidata RAVE or VEEVA

      • Read understand requirement documents/Specifications, database design. Reports design and conduct quality control processes including database review to meet client requirements.

      • Produce Define XML/pdfs, annotated ECRFs and Reviewers Guide for submission deliverables.

      • Develop visual analytics dashboard using tools like Spotfire/Tableau.

      • Perform any post-production changes, publish checks, complex structure dynamics, Rave Safety Gateway, Balance (RTSM) mapping setting to the EDC database or enhancements to the programs like edit checks, listings, Protocol Deviations, etc.

      • Complete assigned work utilizing EDC tools or other proprietary software according to Fortrea sops, Work Instructions and Instructions, project, and project specific guidelines in accordance with Good Clinical Practices.

      • Train and mentor, the team on EDC tools as required and have them ready to perform independent enough on day-to-day activities.

      • Plan, execute and oversee all programming activities on a study, including but not limited to, resource estimation, meeting timelines, maximizing quality, interaction with other departments and the client, etc.

      • Develop/Validate programming specifications for generation of datasets as per Client/CDISC standards.

      • Program edit checks/quality checks on source data and communicate data issues to data management.

      • Perform quality check and ensure the work is delivered with quality and with knowledge of regulations pertaining to computerized systems to ensure compliance.

      • Continuously learn and improve communication, technical and problem-solving skills.

      • Interact with project team members in related discipline and provide solutions to the operational issues.

      • Able to work independently on multiple sponsors and take initiative to accept new challenges in Clinical Programming Applications.

      • Reconcile database build, project files, reports, listings, and other documents related to programming for accuracy, completeness of Data Management processes.

      • Work in a timely manner in accordance with all the activities specified in the agreed study budget, under the supervision of Sr. Programmers.

      • Perform other duties as assigned by Manager.

      Qualifications (Minimum Required):

      • University / college degree (life sciences, health sciences, information technology or related subjects preferred).

      • Experience and/or education plus relevant work experience, equating to a bachelor's degree will be accepted in lieu of a bachelor’s degree.

      Experience (Minimum Required):

      • 4 - 7 years of relevant work experience with a minimum of 2 years of experience in protocol interpretation and study build

      • Good problem-solving skills and a proactive approach.

      • Good oral and written communication skills.

      • Good knowledge of clinical trial process and data management, biometrics, and systems applications to support operations preferred.

      • Ability to work in a team environment.

      • Ability to work effectively under minimal supervision.

      • Ability to prioritize work and Self-motivation.

      • Good time management skills and the ability to work to tight deadlines whilst maintain the highest standards of quality work.

      • A cooperative and team-oriented approach.

      Preferred Qualifications Include:

      • University / college degree (life sciences, health sciences, information technology or related subjects preferred).

      Physical Demands/Work Environment:

      • Home based

      Learn more about our EEO & Accommodations request here.

      Am I A Good Fit?
      beta
      Get Personalized Job Insights.
      Our AI-powered fit analysis compares your resume with a job listing so you know if your skills & experience align.

      The Company
      HQ: Research Triangle Park, NC
      10,811 Employees

      What We Do

      Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development and patient access solutions to the life sciences industry. We partner with emerging and large biopharmaceutical, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients in need. Fortrea provides phase I-IV clinical trial management, clinical pharmacology, differentiated technology-enabled trial solutions and post-approval services. Fortrea’s solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network. Our talented and diverse team working in more than 90 countries is scaled to deliver focused and agile solutions to customers globally. Learn more about how Fortrea is becoming a transformative force from pipeline to patient at Fortrea.com.

      Similar Jobs

      Celonis Logo Celonis

      Territory Partner Manager (Mumbai)

      Big Data • Information Technology • Productivity • Software • Analytics • Business Intelligence • Consulting
      Remote or Hybrid
      India
      3000 Employees

      Bounteous Logo Bounteous

      Manager, Global Compliance and Corporate Governance

      Agency • Digital Media • eCommerce • Professional Services • Software • Analytics • Consulting
      Remote or Hybrid
      India
      5000 Employees
      10-10 Annually

      Nexthink Logo Nexthink

      Finance Manager

      Artificial Intelligence • Big Data • Cloud • Information Technology • Machine Learning • Software
      Remote or Hybrid
      Bengaluru, Karnataka, IND
      1200 Employees

      GitLab Logo GitLab

      Senior Back-end Engineer

      Cloud • Security • Software • Cybersecurity • Automation
      Easy Apply
      Remote
      India
      2500 Employees

      Similar Companies Hiring

      Formation Bio Thumbnail
      Artificial Intelligence • Big Data • Healthtech • Biotech • Pharmaceutical
      New York, NY
      140 Employees
      SOPHiA GENETICS Thumbnail
      Software • Healthtech • Biotech • Big Data • Artificial Intelligence
      Boston, MA
      450 Employees
      Pfizer Thumbnail
      Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
      New York, NY
      121990 Employees

      Sign up now Access later

      Create Free Account

      Please log in or sign up to report this job.

      Create Free Account