Senior Manager, Clinical Trial Analyst

Summit, NJ US
Competitive Salary
Oct 18, 2016
Nov 15, 2016
Result Type
Position Type
Full Time


Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health.  We value our passion for patients, quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries - and growing we look for talented people to grow our business, advance our science and contribute to our unique culture.

Summary/Scope :  Supports and interacts with Clinical Research & Development Operations (CR & D Operations) Functional Leadership in the development and validation of feasibility criteria for clinical programs/studies, timeline projection and study specific recruitment and retention strategies inclusive of scenario modeling according to study specific assumptions. 

Responsibilities will include, but are not limited to, the following:

Clinical Trial Strategies and Analytics

•Collaborate with Clinical Research and Development Operations functions and cross-functional areas to create clinical trial process modeling focused on study planning and enrollment to drive optimal decision making and management of study risks.

•Lead development of feasibility criteria for clinical programs/studies, timeline projection and study specific recruitment and retention strategies

•Collaborate with Clinical Research and Development Operations functions and cross-functional areas to identify, collect, integrate and analyze internal and external data sets that may better enable the  projection of program/study milestones, identification of  potential countries and sites, and facilitate  subject recruitment and retention strategies and tactics.

•Engages with Regulatory, Commercial and other Celgene functions who evaluate Epidemiological data for the purposes of identifying incidence and prevalence of targeted patient population, inclusive of identifying global vs. regional/local standards of care that must be considered.   

•Participate in early identification of potential risks to objectives above and contributes to the development of risk specific contingency plans to promote proactive remediation. 

•Participate in root cause analysis and developing and implementing mitigation strategies when needed.  

•Develop and recommend program and study level recruitment and retention plans.

•Collaborates with Clinical Operations to develop program/study level subject recruitment and retention strategies. 

•Conducts operational analysis and planning to ensure that subject recruitment strategies and tactics identified for a program/study are practical, experienced based and cost effective to execute, inclusive of identification, evaluation, selection and oversight of recruitment vendors.

•Works with local affiliates to ensure compliance with federal and country/local regulations regarding study start up and enrollment strategies.  

•Provides project management for the implementation of subject recruitment and retention strategies related to recruitment and media vendors including timelines and budget.  

•Participates in root cause analysis and makes adjustments to retention/recruitment planning. 

•Responsible for identifying, assessing, introducing and ensuring the application of innovative techniques and tools that enable a data driven country/site selection and subject recruitment/retention processes.

•Analyzes and identifies trends, variations, successfully demonstrated practices, potential problems and opportunities for process improvement.

•Identifies opportunities and fosters collaboration and partnership within organization.  Drive Therapeutic Area or function specific interactions with external vendors such as CROs, Investigator networks, Site Management Organizations, hospital or university clinical research units, advocacy groups and recruitment vendors.

•Identifies and supports the use of industry leading tools/templates/systems that enable those processes associated with Protocol Design, industry benchmarking, Project Management, Scenario modeling and probability.

•Participates in and/or oversees retrospective analysis of issues to determine what happened, how many, how often, where the problem is, and what actions are needed within Clinical Research and Development Operations functions and other cross-functional areas.  



•BA/BS or equivalent degree preferably in life sciences or allied health field •At least 5-10 years career experience including 3-5 years of experience in CR & D Operations roles 

Skills/Knowledge Required: ?BA/BS or equivalent degree preferably in life sciences or allied health field.          Degree in mathematics /statistics and life sciences highly desirable. ?Familiarity, and preferably proven mastery, of Simulation/Modeling/Algorithm        /Forecasting capabilities to enable the creation and management of trial             scenario planning, data analytics and correlation analyses using Statistical         Methods. ?Experience with the global drug development process/management of clinical      studies and current knowledge of GCP/ICH Guidelines and Regulations. ?Advanced Clinical Trial Planning & Execution experience/expertise. ?Analytical mindset with attention to detail. ?Demonstrated administrative and project management abilities in relevant            clinical development setting. ?Demonstrated experience managing and collaborating in a team/matrix work      environment.  Ability to direct activities and influence outcomes without direct      authority.  Ability to work independently. ?Good verbal, written and interpersonal skills – communication and                        presentation skills demonstrated in an international clinical                                    research environment. ?Familiarity with process improvement methodologies (e.g. Six Sigma, Lean) a      plus. ?Computer and systems literate; familiarity with Microsoft Office programs,            including Microsoft Project, WORD, Excel, PowerPoint, SharePoint,                Livelink, etc. Familiarity with Minitab or other Statistical computing software  is    highly desired.

Celgene is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.

Celgene complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must have authorization to work for Celgene in the U.S.