Sr Manager, Central Monitoring

Posted 7 Days Ago
Be an Early Applicant
Hiring Remotely in United States
Remote
130K-212K Annually
7+ Years Experience
Biotech • Pharmaceutical
The Role
The Senior Manager, Central Monitoring is responsible for centralized monitoring activities for global and/or complex trials, analytical data review, interpretation of Key Risk Indicator (KRI) and Key Performance Indicator (KPI) data, presenting findings, and driving process improvement in central monitoring capabilities.
Summary Generated by Built In

The Senior Manager, Central Monitoring is accountable for centralized monitoring activities for global and/or complex trials or program level analytical data review of key risk and/or operational performance data and presenting as an integral member of the Clinical Study team for clinical development studies. The reviews include interpretation of Key Risk Indicator (KRI) and/or Key Performance Indicator (KPI) data housed in an analytical tool as well as a Comprehensive review of supplemental operational data/trends and issues to be interpreted, reported and presented to the study teams. The Senior Manager, Central Monitoring will be responsible for supporting a number of studies within a therapy area and program-level. They will work closely with other Central Monitors to ensure effective identification, conduct and reporting of central monitoring activities in support of sponsor oversight obligations. The role will lead, contribute, and drive continued process improvement and innovation activities, and industry collaborations in central monitoring capabilities.

A typical day in this role looks like:

Central Monitoring Reviews

  • Responsible for development and authoring activities of the Central Monitoring Plan
  • Participate in the Quality Risk and Control Tracker (QRACT) development
  • Present at the CRO kick-off meeting
  • Work with data analysts in the technical configurations, implementation, and execution of Central Monitoring RBQM system, Cluepoints, across studies.
  • Conduct & Communicate Study-level and Program-Level Central Monitoring Review for assigned studies in a given program/therapeutic area using data analysis tools
  • Interpret the relationships between each Key Performance Indicator/metric and any supporting data to critically assess trends within a site/study
  • Review, interpret and report data as an integral part of the Clinical Study Team in support of identifying centralized monitoring activities and/or investigator sites potentially requiring sponsor intervention.
  • Support study teams in understanding the impact, criticality and potential root causes of the findings and defining appropriate follow-up actions.
  • Document the output from the Central Monitoring Review meetings and track decisions/actions to closure
  • Access, review and complete applicable tracking and reporting tools when necessary eg. CTMS/ODR/etc.

Risk-Based Quality Management Methodology

  • Define strategies, interpret data, and provide insights for Central Monitoring under the Risk-Based Quality Management (RBQM) operating model at functional and partnership levels.
  • Present at periodic study and program-level Quality Risk Review meetings with the study team
  • Act as a subject matter expert for the implementation and execution of Central Monitoring within the study teams
  • Represent Central Monitoring with audit and inspection preparation and conduct if applicable

Functional Oversight

  • Partner with outsourcing management and counterparts at CROs to align on monitoring and central monitoring strategy, standards, risk based monitoring strategy, and input into the central monitoring documents
  • Provide oversight of CRO partner central monitoring activities ensuring the CRO is executing per the Partnership Operations Manual

Continuous Improvement

  • Critically evaluate the availability, quality and output of integrated data, metrics and reports to ensure they continue to meet the needs in support of the Central Monitoring review processes
  • Represent Central Monitoring in process improvement initiatives, and participate in functional strategic planning
  • Assess and evaluate the Central Monitoring Process including sensitivity of detection methods, availability of new technologies, required enhancements to process
    to further refine where necessary
  • Assign and delegate appropriate tasks to Central Monitoring Associate Manager & Central Monitoring Managers
  • Line management and performance management; Tasks include and are not limited to: raising/setting/communicating performance standards; performing ongoing performance management activities including individual goal setting/periodic performance assessments/timely performance feedback/coaching/development planning; and tracking and monitoring attendance/timesheets/expense reports.
  • May require 25% travel

In order to be considered qualified for this role, a minimum of a BS degree and 8+ years of relevant industry related experience is required. Direct hands on experience in Cluepoints is required

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.

For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.

Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.

Salary Range (annually)

$129,800.00 - $211,800.00

Top Skills

Cluepoints
The Company
HQ: Rensselaer, New York
15,000 Employees
Hybrid Workplace
Year Founded: 1988

What We Do

At Regeneron we believe that when the right idea finds the right team, powerful change is possible. As we work across our expanding global network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to think about science, manufacturing and commercialization. And new ways to think about health. Connect with us so we can learn more about you, and you can learn more about our biopharmaceutical medicines. And join us, as we build a future we believe in.

Please visit www.regeneron.com/social-media-terms for information on how to engage with us on social media.

An important note about privacy: Regeneron is committed to your privacy and will not ask for sensitive personal information such as social security number, date of birth or bank account details via email or social media.

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