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Associate Director, Monitoring Services Oversight Management

Band

Level 5


 

Job Description Summary

About the role:
#LI-Remote

Primary contact for Full-Service Provider (FSP) and other monitoring services (vendors) to assure adequate quality of the services & performance in Novartis sponsored clinical trials. Oversees vendor monitoring performance targets per defined quality performance indicators, including site recruitment commitments, timely data entry and issue resolution Key Performance Indicators (KPIs). Aligns with FSP and other vendor’s managers on Clinical Research Associate and other vendor resource related allocation to trials and studies.


 

Job Description

Key Responsibilities:

  • Ensures timely communication with vendors’ line managers to ensure sponsor requirements are up to date – sets up governance model
  • Develop resource needs/expectations strategy and align with vendor line management (CRAs and other vendor resources)
  • Collaborates with Clinical Research Associate (CRA) Manager and other internal stakeholders for country resource strategy to be best single point of contact/ primary interface FSP/other vendors
  • Promotes a compliance culture advocating the adherence to highest standards and ethical integrity, ensuring human subject protection and reliability of trial results at all times
  • Escalates non-compliance, performance issues, competency gaps and/or needs to vendors
  • Oversees country trial site activation, enrolment, data flow and timeline commitments are delivered per established trial objectives
  • Oversees monitoring quality, timely data entry and issue resolution including oversight of CRA oversight visit performance
  • Oversee execution of annual CRA oversight visit plan to assess vendor issue management and oversight in close collaboration with FSP line management

Essential Requirements:

  • This position can be based remotely anywhere in the U.S. (there may be some restrictions based on legal entity). Please note that this role would not provide relocation as a result. The expectation of working hours and travel (domestic and/or international) will be defined by the hiring manager. This position will require 30-40% travel.
  • A degree in scientific or health discipline required and advanced degree preferable (or, for United States: 4-year degree plus relevant, related healthcare experience).
  • Minimum 7 years of experience in clinical research planning/executing and/or monitoring clinical trials.
  • Experience and evidence of team leadership capabilities.
  • Understanding all aspects of clinical drug development with particular emphasis on monitoring and trial execution.
  • Fluent in both written and spoken English.
  • Strong communication skills and ability to influence internal and external stakeholders in order to maximize quality and efficiency of external service providers.

Novartis Compensation and Benefit Summary: The pay range for this position at commencement of employment is expected to be between: $145,600 and $270,400/year; however, while salary ranges are effective from 1/1/25 through 12/31/25, fluctuations in the job market may necessitate adjustments to pay ranges during this period.  Further, final pay determinations will depend on various factors, including, but not limited to geographical location, experience level, knowledge, skills, and abilities. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.


 

EEO Statement:

The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential.


 

Accessibility and reasonable accommodations

The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an e-mail to tas.nacomms@novartis.com call +1 (877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

https://www.novartis.com/careers/careers-research/notice-all-applicants-us-job-openings



 

Salary Range

$145,600.00 - $270,400.00


 

Skills Desired

Budget Management, Clinical Monitoring, Clinical Research, Clinical Study Reports, Clinical Trials, Collaboration, Data Analysis, Decision Making Skills, Health Sciences, Lifesciences, People Management, Regulatory Compliance
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Average salary estimate

$208000 / YEARLY (est.)
min
max
$145600K
$270400K

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What You Should Know About Associate Director, Monitoring Services Oversight Management, Novartis

Are you ready to take the next step in your career? As the Associate Director of Monitoring Services Oversight Management at Novartis, you’ll play a pivotal role in ensuring the success of our clinical trials from a remote position anywhere in the U.S. In this dynamic role, you will be the primary contact for our Full-Service Provider and other monitoring services vendors, working tirelessly to maintain the highest quality standards for trial performance. You will be involved in aligning resources, overseeing trial site activation, and ensuring data flows smoothly. You’ll set expectations, manage key performance indicators, and be an advocate for compliance and ethical integrity in all aspects of clinical research. Collaborating with various stakeholders, you’ll drive outcomes through strategic resource planning and performance management. We're looking for someone with at least 7 years of critical experience in clinical research who is fluent in English and possesses excellent communication skills. At Novartis, you can expect a competitive compensation package starting from $145,600/year, which could go up to $270,400/year depending on your experience and skills. Join us if you're eager to contribute to groundbreaking research while working remotely with travel opportunities!

Frequently Asked Questions (FAQs) for Associate Director, Monitoring Services Oversight Management Role at Novartis
What are the key responsibilities of an Associate Director, Monitoring Services Oversight Management at Novartis?

As the Associate Director of Monitoring Services Oversight Management at Novartis, you will oversee monitoring performance targets, ensure compliance with sponsor requirements, and manage vendor communications. Your primary aim will be to evaluate resource allocation, manage country trial site activities, and promote a culture of high ethical standards and human subject protection.

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What qualifications are required for the Associate Director, Monitoring Services Oversight Management position at Novartis?

To qualify for the Associate Director position at Novartis, candidates must possess a degree in a scientific or health discipline, preferably an advanced degree. A minimum of 7 years of clinical research experience in planning, executing, or monitoring trials is essential, along with demonstrated leadership capabilities and proficiency in English.

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How does Novartis support career growth for the Associate Director, Monitoring Services Oversight Management role?

At Novartis, as an Associate Director of Monitoring Services Oversight Management, you will have access to various career development opportunities, including mentorship and leadership training programs. The company's commitment to innovation and employee development ensures that you can continuously grow and advance your career while working on exciting clinical research projects.

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What travel expectations are associated with the Associate Director, Monitoring Services Oversight Management position at Novartis?

The Associate Director role at Novartis requires approximately 30-40% travel, which may be both domestic and international. Travel is essential to fulfill responsibilities related to vendor management and overseeing clinical trial activities effectively.

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What is the expected salary range for the Associate Director, Monitoring Services Oversight Management position at Novartis?

The salary range for the Associate Director, Monitoring Services Oversight Management position at Novartis ranges from $145,600 to $270,400 per year, depending on various factors such as experience level, skills, and geographical location. Additionally, the total compensation package may include a sign-on bonus and other benefits.

Join Rise to see the full answer
Common Interview Questions for Associate Director, Monitoring Services Oversight Management
What strategies would you implement for ensuring compliance in clinical trials as an Associate Director?

In answering this question, focus on your approach to build a compliance culture, emphasize the importance of training for all team members on ethical practices, and describe how regular audits and KPIs would be used to monitor adherence. Discuss prior experiences where compliance measures led to successful trial outcomes.

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How do you manage vendor relationships in clinical research?

Talk about your experience in fostering strong communication and collaboration with vendors, establishing clear expectations and performance metrics. Give examples of how you have addressed performance issues, enhancing partnerships through guidance and support.

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Describe a challenging situation you faced in clinical trial management and how you resolved it?

Choose a specific example where you encountered a significant challenge, such as data discrepancies or recruitment issues. Explain the steps you took to analyze the problem, collaborate with your team and stakeholders, and implement a solution that led to improved outcomes.

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What metrics do you consider critical when evaluating the performance of clinical trial vendors?

Discuss specific Key Performance Indicators (KPIs) you prioritize, such as site recruitment rates, data entry timelines, and issue resolution efficiency. Illustrate how you use these metrics to ensure quality service and adherence to trial objectives.

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How do you prioritize your responsibilities when overseeing multiple clinical trials?

Highlight your organizational skills and ability to manage time effectively. Discuss using project management tools to prioritize tasks based on urgency and importance while ensuring that team members are aligned with overall trial goals.

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What do you believe are the essential skills for an Associate Director in Monitoring Services Oversight Management?

Mention key skills such as strong communication abilities, strategic thinking, data analysis, and leadership qualities. Explain how these skills contribute to effective vendor management and successful trial execution.

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How would you handle a situation where a vendor is not meeting performance expectations?

Explain the importance of addressing issues promptly and how you'd initiate a discussion with the vendor to understand the root cause. Discuss possible resolutions you would explore, including providing additional support or realigning expectations.

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In your experience, what makes a successful clinical trial team?

Reflect on factors like effective communication, mutual respect, and clearly defined roles within the team. Provide specific examples of how fostering these factors contributed to previous trial successes.

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Can you provide an example of how you've influenced stakeholders regarding clinical trial outcomes?

Share a specific instance where you successfully advocated for a change or infusion of resources. Discuss the data or persuasive arguments you used to gain buy-in from stakeholders.

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What is your approach to professional development and keeping up-to-date with clinical research trends?

Talk about your commitment to lifelong learning, whether through attending conferences, participating in webinars, or pursuing additional qualifications relevant to clinical research. Emphasize how staying informed enhances your effectiveness in the Associate Director role.

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Our purpose is to reimagine medicine to improve and extend people's lives. We use innovative science and technology to address some of society's most challenging healthcare issues. We discover and develop breakthrough treatments and find new ways ...

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Full-time, remote
DATE POSTED
March 29, 2025

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