Data Management Sr Associate

Biopharma Careers; Hyderabad; On-site; INR 2,000,000 - 3,200,000; Full time

Benefits offered by this job

Total rewards plan

Remote work possible

Competitive benefits

Job summary

Amgen is seeking a Sr Data Management Support in Hyderabad to help deliver high-quality clinical trial data across the study lifecycle. You will execute data management tasks, support data delivery leads and coordinate with cross-functional teams to ensure compliant, timely study execution.

The role requires a Master’s or Bachelor’s with clinical execution experience, 3 years in life sciences, and experience in data management on global trials.

Qualifications

• Master’s degree or Bachelor’s degree with clinical execution experience
• 3 years’ work experience in life sciences or related field, including 1 year in clinical trials
• Experience in Data Management on global clinical trials

Responsibilities

• Support delivery of high-quality clinical trial data across the study lifecycle
• Execute data management tasks including database build testing, data cleaning, query management, reconciliation and lock preparation
• Coordinate with internal and external teams to ensure timely, compliant study delivery

Skills

Clinical data management

Life sciences experience

Global trials experience

Education

Master’s degree

Bachelor’s degree

Associate’s degree

High school diploma

Tools

EDC databases

Data dictionaries

Job description

Career Category

Clinical Development

Job Description

Join 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.

Sr Data Management Support

What you will do

• Let’s do this. Let’s change the world. In this vital role you will support the delivery of high-quality clinical trial data by executing core data management activities across the study lifecycle, ensuring data integrity, compliance, and timely study execution.
• Execute study data management tasks including database build testing, data cleaning, query management, reconciliation, and lock preparation with limited oversight
• Support core Data Management roles, such as Data Delivery Leads, Database Designers, and Data Acquisition Leads by owning time-sensitive deliverables with high-quality execution
• Actively c ontribute to setup and maintenance of EDC/non CRF data structures including local labs, coding dictionaries, along with non-CRF data integrations
• Track progress against data management timelines, study timelines and deliverables, identify risks or delays, and elevate issues with clear documentation and any mitigations
• Coordinate with local internal teams, global team members as well as external partners (including FSPs) when required to ensure aligned and efficient delivery of all study activities
• Identify opportunities to improve repeatable processes and contribute to best practices and knowledge sharing across the team

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The candidate we seek is an individual with the following qualifications.

• Master’s degree OR
• Bachelor’s degree and 2 years of clinical execution experience OR
• Associate’s degree and 6 years of clinical execution experience OR High school diploma / GED and 8 years of clinical execution experience

• 3 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 working in Data Management on global clinical trials

What you can expect of us

As 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 plan
• Stock-based long-term incentives
• Award-winning time-off plans and bi-annual company-wide shutdowns
• Flexible work models, including remote work arrangements, where possible

As 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.