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Database Design Associate

Amgen

Database Design Associate

full-timePosted: Jul 29, 2026Updated: Aug 28, 2026India - Hyderabad

Job Description

Career CategoryClinical DevelopmentJob DescriptionJoin Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.Data Management SupportWhat you will doLet’s do this. Let’s change the world. In this vital role you will support the execution of core data management activities across the clinical trial lifecycle, ensuring high-quality, timely, and compliant data delivery to enable effective study outcomes and decision-making.Support execution of core data management activities across the study lifecycle, including database build, edit check testing, lab and coding setup, data cleaning, query management, reconciliation, and lock preparation.Provide hands-on, flexible support across build, conduct, and closeout phases, developing broad exposure to end-to-end data management processes and study delivery.Deliver accurate and timely completion of assigned tasks, eg query management in support of Data Delivery.Assist in the preparation and maintenance of study documentation, including CRF testing scripts, reconciliation trackers, and lock readiness materials.Monitor data quality and query trends, proactively identifying issues, escalating where appropriate, and contributing to practical solutions.Collaborate cross-functionally when required, building proficiency in EDC systems (e.g., Veeva Vault, Medidata Rave) and other data management tools.What we expect of youWe are all different, yet we all use our unique contributions to serve patients. The candidate we seek is an individual with the following qualifications.Basic Qualifications:Bachelor’s degree ORAssociate’s degree and 4 years of clinical execution experience ORHigh school diploma / GED and 6 years of clinical execution experiencePreferred Qualifications:2 years' work experience in life sciences or medically related field, including 1 years of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO companyExperience working in Data Management on global clinical trialsWhat you can expect of usAs we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.A discretionary annual bonus program, or for field sales representatives, a sales-based incentive planStock-based long-term incentivesAward-winning time-off plans and bi-annual company-wide shutdownsFlexible work models, including remote work arrangements, where possibleApply nowfor a career that defies imaginationObjects in your future are closer than they appear. Join us.careers.amgen.comAs an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation..

Locations

  • India - Hyderabad

Skills Required

  • life sciencesintermediate

Required Qualifications

  • Bachelor’s degree OR (degree)
  • Associate’s degree and 4 years of clinical execution experience OR (experience, 4 years)
  • High school diploma / GED and 6 years of clinical execution experience (experience, 6 years)

Preferred Qualifications

  • 2 years' work experience in life sciences or medically related field, including 1 years of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company (experience, 2 years)
  • Experience working in Data Management on global clinical trials (experience)

Responsibilities

  • Let’s do this. Let’s change the world. In this vital role you will support the execution of core data management activities across the clinical trial lifecycle, ensuring high-quality, timely, and compliant data delivery to enable effective study outcomes and decision-making.
  • Support execution of core data management activities across the study lifecycle, including database build, edit check testing, lab and coding setup, data cleaning, query management, reconciliation, and lock preparation.
  • Provide hands-on, flexible support across build, conduct, and closeout phases, developing broad exposure to end-to-end data management processes and study delivery.
  • Deliver accurate and timely completion of assigned tasks, eg query management in support of Data Delivery.
  • Assist in the preparation and maintenance of study documentation, including CRF testing scripts, reconciliation trackers, and lock readiness materials.
  • Monitor data quality and query trends, proactively identifying issues, escalating where appropriate, and contributing to practical solutions.
  • Collaborate cross-functionally when required, building proficiency in EDC systems (e.g., Veeva Vault, Medidata Rave) and other data management tools.

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