Analyst, Evidence Generation Data Management

Join a Legacy of Innovation 125 Years and Counting!

Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 125 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and its 18,000 employees around the world draw upon a rich legacy of innovation and a robust pipeline of promising new medicines to help people. In addition to a strong portfolio of medicines for cardiovascular diseases, under the Group’s 2025 Vision to become a “Global Pharma Innovator with Competitive Advantage in Oncology,” Daiichi Sankyo is primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders.   

SUMMARY

• The position holder will support end-to-end delivery of data management services for assigned studies, collaborating with CROs and other vendors to ensure high quality deliverables are on time and within budget.
• The position holder will support the study lead and partner with internal and external stakeholders to optimize Data Management technology, processes, and standards.
• The position will understand Electronic Data Capture/related applications and industry standards, and fundamental technical skills in working with data received from CROs and other third-party vendors.

RESPONSIBILITIES

Study Responsibilities:

• Responsible, with strict supervision, for study activities assigned related to the Data Management study set up, conduct, and close out
• Ensure timely, to budget and accurate completion of Data Management deliverables, including but not exclusive to the Data Management Plan, Database specifications, Database build, interim data cuts, Database lock and study archiving
• Must comply with international regulations, with guidance under Manager
• Ensure inspection readiness, as well as prepare potential audits linked to assigned studies

Vendor Oversight:

• With supervision, responsible for routine oversight of vendor delivery, to ensure compliance with the protocol, external/internal standards applicable regulatory guidelines, Policies, SOPs, and other relevant guidelines.

Operational Excellence:

• Participate, with supervision, in Global Evidence Generation initiatives to improve the harmonization and efficiency of processes and/or develop and implement innovative solutions
• Maintains current knowledge of industry best practice in Data Management methodology, Data Integrity, and Data Privacy
• Any other supporting duties deemed pertinent to the needs of the business (included but not limited to: town halls meetings coordination)

Qualifications: Successful candidates will be able to meet the qualifications below with or without a reasonable accommodation.

Education Qualifications (from an accredited college or university)

• Bachelor's Degree Related Sciences required

Experience Qualifications

• Must have a minimum of at least 1 or more years of professional pharmaceutical industry experience, or other related healthcare experience (i.e, CRO) with experience related to study activities assigned related to data management, study set up, conduct, and close out.
• Must have proven expertise experience supporting post marketed drug development in either the pharmaceutical industry or within CRO.

Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.