Job added in hotlist
Applied job
Contract job
90-day-old-job
part-time-job
Recruiter job
Employer job
Expanded search
Apply online not available
Similar Jobs
Clerical Assistant
Confidential
, NY
Apply Now >
Administrative Assistant
KST Realty
New York City, NY
Apply Now >
Admin Assistant
Performance Signs & Graphics
New York City, NY
Apply Now >
Paralegal
New York City, NY
Apply Now >
Administrative Staff
New York City, NY
Apply Now >
View more jobs in Berkeley Heights, NJ
View more jobs in New Jersey

Job Details

Senior Manager Rave Global Librarian

Company name
Bristol-Myers Squibb Company

Location
Berkeley Heights, NJ, United States

Employment Type
Full-Time

Industry
Administrative, Library

Posted on
Apr 01, 2020

Apply for this job






Profile

Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis.

Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results.

The Senior Manager, Rave Global Librarian is a role considered essential to the sustainability and success of the BMS R&D pipeline. This role reports to the Associate Director – Central Build Group, Clinical Data Acquisition & Standards within the Global Data Management and Centralized Monitoring (GDMCM) function of Global Development Operations (GDO).

Responsibilities Include

Building, maintaining and documenting the global library objects in order to facilitate the creation of Study Level databases to collect clinical trial data.

Working with the Data Managers – Study Start Up and Database Developers to implement new or modified global library objects.

Building, maintaining and documenting the Safety Gateway related objects in order to facilitate the creation of Study Level databases and mappings to collect clinical trial data and transmit this data to the Aware System and manage the Safety Gateway Management Tool.

Managing work assignments to ensure timely delivery of global library objects.

Working with Data Managers – Study Start Up, Global Standards and the Custom Function Programmers to develop appropriate timelines for development and deployment of global library objects.

Identifying and resolving issues which may negatively impact delivery of global library objects. Escalating issues to leadership as needed.

Following procedural documents and participating in reviewing and updating documents to make sure they are reflective of industry standards and easily followed.

Contributing to the development and application of smart systems and optimal approaches to support the collection of data.

Actively participating in and/or leading continuous improvement activities, defining and implementing the changes required to create an industry-leading electronic data capture capability.

Liaising with and reviewing work delivered by external partners (e.g. Function Service Providers, CROs, technology providers, etc.) performing Central Build Group services on behalf of BMS.

Developing strong and productive working relationships with key stakeholders throughout GDMCM, GDO, and BMS with the ability to think strategically across a broad portfolio and effectively express his/her views to senior management.

Representing the Company in interactions with key external partners as part of any committee or industry group relating to Central Build Group.

Some Senior Managers may also be responsible for managing employees and/or Functional Service Providers - Reviewing deliverables and timelines, providing ongoing feedback and performance review, empowering and holding staff to high quality performance and delivery.

Experience and Expertise Required

Bachelor’s degree required with an advanced degree preferred. At least 5 years of relevant industry experience. Project management certification (e.g. PMP) is desirable.

At least 5 years of database developer experience in Rave with experience of Global Libraries and standards.

Global clinical trial expertise and a successful track record of leading through influence, working across complex, global organizational matrices. Immuno-Oncology therapeutic experience is highly desirable.

Good understanding of the drug development process with proven expertise in clinical trial execution and data acquisition in a global arena.

Strong knowledge of industry leading eCRF tools (e.g. Medidata Rave, Oracle, etc.) and well versed in industry trends and emerging technologies supporting data collection.

Strong knowledge of GCP/ICH guidelines.

Technical expertise, technical writing ability, and proficiency in Systems Development LifeCycle (SDLC) principles.

An understanding of database and dictionary structures (e.g. MedDRA, WHODrug).

Demonstrated partnership across various collaborative forums, CROs, SMOs and/or local site networks.

Diverse and sufficient technical expertise to be a credible interface to all global development and business partners (medical, development, commercial, regulatory & quality etc.).

Influential leadership and communication capabilities with a proven ability to engage, manage, develop and inspire a geographically diverse team.

This is a full-time, office-based position located in Central New Jersey.

Bristol-Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees the resources to pursue their goals, both at work and in their personal lives.

Bristol-Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

Company info

Bristol-Myers Squibb Company
Website : http://www.bms.com

Similar Jobs:
paralegals
Location : Edison, NJ
Our firm has ten office locations throughout Central New Jersey. We are often seeking talented, energetic and experienced candidates to fill various staff positions. This may include: attorneys, paralegals, law clerks, legal assis...
Office Clerical
Location : New York City, NY
Basic office activities including but not limited to: filing, sorting paperwork and data entry.
Legal Administrative Assistant
Location : New York City, NY
New York Wiggin and Dana is looking for a Legal Administrative Assistant to support busy lawyers in our New York City location. The ideal candidate works well under pressure, is able to prioritize assignments, multitask, have fant...
I like the volume of jobs on EmploymentCrossing. The quality of jobs is also good. Plus, they get refreshed very often. Great work!
Roberto D - Seattle, WA
  • All we do is research jobs.
  • Our team of researchers, programmers, and analysts find you jobs from over 1,000 career pages and other sources
  • Our members get more interviews and jobs than people who use "public job boards"
Shoot for the moon. Even if you miss it, you will land among the stars.
AdminCrossing - #1 Job Aggregation and Private Job-Opening Research Service — The Most Quality Jobs Anywhere
AdminCrossing is the first job consolidation service in the employment industry to seek to include every job that exists in the world.
Copyright © 2024 AdminCrossing - All rights reserved. 168 192