Senior Manager, Data Management

Reposted 19 Days Ago
Be an Early Applicant
Nutley, NJ, USA
In-Office
135K-177K Annually
Senior level
Healthtech • Pharmaceutical • Manufacturing
The Role
Manage clinical data activities from study start-up through completion, develop eCRFs/DMPs/validation and data transfer specs, oversee CROs and internal teams, ensure GCP/SOP/regulatory compliance, represent Data Management on study teams, mentor staff, and deliver quality data.
Summary Generated by Built In

At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai’s human health care (hhc) mission. We’re a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, notably the discovery of the world's most widely-used treatment for Alzheimer’s disease. As we continue to expand, we are seeking highly-motivated individuals who want to work in a fast-paced environment and make a difference.  If this is your profile, we want to hear from you.

The Sr. Manager Data Management is primarily responsible for the direct management of clinical study activities as they relate to data collection and processing from study start up through ongoing oversight to completion. Working in a highly matrixed environment, the successful candidate must have proven ability to effectively manage outsourced vendor activities as well as internal resources. The candidate must be capable of managing and leading others, providing appropriate feedback when warranted, setting clear direction for team members and appropriately assigning resources to meet work objectives. This individual may also act as “compound lead” for select projects to ensure consistency in the DB build across all protocols, ensuring conformity to Eisai standards.

Responsibilities:

  • Develop and review standard Case Report Forms (eCRFs), Data Management Plan, Validation Specifications and Data transfer Specifications.
  • Provide Data Management inputs during study protocol development; contribute to the enhancement of a clinical library.
  • Participate in the development/maintenance of DM SOPs, Standard Working Practices, and other data management related process documents as needed.
  • As appropriate, contribute to the selection, oversight of CRO performance related to Data Management activities; act as the sponsor representative for data management outsourced activities.
  • Represent the Data Management function in study teams meetings.
  • Ensure timely delivery of quality data in accordance with Eisai's SOP, industry standards, and regulatory guidelines.
  • Work closely with cross functional teams to ensure delivery of quality data; represent Data Management team in study team meetings and provide Data Management questions to internal and external team members.
  • Execute managerial duties to direct reports and/or provide guidance to members.

Qualifications:

  • Bachelors degree in sciences or related field  with 7+ years of clinical data management experience in pharma/biotech industry OR a combination of equivalent education and experience.
  • Experience in project management (i.e. defining plans and milestones, coordinating with cross functional teams and driving accountabilities).
  • Experience working with clinical trials and the drug development process; understanding of Data Management strategy.
  • Experience leading data management activities in clinical trials.
  • Proficient use of data management systems with strong knowledge of data management processes, tools, methodologies and documentation.
  • Strong experience and knowledge of clinical research, GCP, regulatory requirements and good data management practices.
  • Some experience with line management; mentoring team members (external/contract staff) on clinical data management activities and procedures preferred.
  • Proven performance in earlier role.
  • Position is hybrid, requiring 3 days onsite per week (Tuesday, Wednesday and Thursday).

#LI-MI1

Skills:Communication & Cross-functional Influence, Critical Thinking & Business Agility, Data Management Knowledge/Skills, Industry/ Regulatory Knowledge, Mentoring/ People Development, Project Management, Vendor Management

Eisai Salary Transparency Language:

The annual base salary range for the Senior Manager, Data Management is from :$134,800-$176,900

Under current guidelines, this position is eligible to participate in : Eisai Inc. Annual Incentive Plan.

Final pay determinations will depend on various factors including but not limited to experience level, education, knowledge, and skills.

Employees are eligible to participate in Company employee benefit programs. For additional information on Company employee benefits programs, visit https://careers.eisai.com/us/en/compensation-and-benefits.

Certain other benefits may be available for this position, please discuss any questions with your recruiter.

Eisai is an equal opportunity employer and as such, is committed in policy and in practice to recruit, hire, train, and promote in all job qualifications without regard to race, color, religion, gender, age, national origin, citizenship status, marital status, sexual orientation, gender identity, disability or veteran status.  Similarly, considering the need for reasonable accommodations, Eisai prohibits discrimination against persons because of disability, including disabled veterans.

Eisai Inc. participates in E-Verify. E-Verify is an Internet based system operated by the Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment eligibility of all new hires in the United States. Please click on the following link for more information:

Right To Work

E-Verify Participation

Skills Required

  • Bachelor's degree in sciences or related field with 7+ years of clinical data management experience in pharma/biotech (or equivalent education/experience).
  • Experience leading data management activities in clinical trials and understanding of Data Management strategy.
  • Experience in project management (defining plans and milestones, coordinating cross-functional teams, driving accountabilities).
  • Proficient use of data management systems and strong knowledge of data management processes, tools, methodologies and documentation.
  • Strong knowledge of clinical research, GCP, regulatory requirements and good data management practices.
  • Experience managing/overseeing outsourced CRO data management activities and acting as sponsor representative.
  • Some experience with line management; mentoring team members (external/contract staff).
  • Position is hybrid, requiring 3 days onsite per week (Tuesday, Wednesday and Thursday).
  • Proven performance in earlier role.

Eisai US Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Eisai US and has not been reviewed or approved by Eisai US.

  • Leave & Time Off Breadth Paid time off starts high at 20–25 days with 12 company holidays, and site-based teams observe Summer Hours for half the year, expanding practical time away from work.
  • Retirement Support The retirement program pairs a 401(k) match with an extra 4%–7% non‑elective contribution based on tenure, boosting savings even without employee contributions.
  • Flexible Benefits Work flexibility includes hybrid and fully remote roles with a $1,000 home‑office technology stipend for eligible new hires, reducing the cost of remote setup.

Eisai US Insights

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The Company
HQ: Nutley, NJ
2,984 Employees
Year Founded: 1985

What We Do

At Eisai Inc., human health care (hhc) is our goal. We give our first thought to patients and their families, and helping to increase the benefits health care provides. As the U.S. pharmaceutical subsidiary of Tokyo-based Eisai Co., Ltd., we have a passionate commitment to patient care that is the driving force behind our efforts to discover and develop innovative therapies to help address unmet medical needs. Eisai is a fully integrated pharmaceutical business that operates in two global business groups: oncology and neurology (dementia-related diseases and neurodegenerative diseases). Each group functions as an end-to-end global business with discovery, development, and marketing capabilities. Our U.S. headquarters, commercial and clinical development organizations are located in New Jersey; our discovery labs are in Massachusetts and Pennsylvania; and our global demand chain organization resides in Maryland and North Carolina. To learn more about Eisai Inc., please visit us at www.eisai.com/US. Comments and posts by users on this site are not created or controlled by Eisai Inc. and Eisai is not responsible for such content

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