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Associate Director Clinical Data Management Jobs in Michigan

... clinical research operations across assigned regions/sites * Support site managers, team leads ... Ensure quality standards across documentation, data entry, and essential files * Participate in ...

Clinical Operations Schedule: Full-time | Day Salary range: $92,493.52 - $125,138.10 per year Life ... management OR Associate's degree/Bachelor's degree with 3 years of applicable cumulative job ...

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Associate Director Clinical Data Management information

See Michigan salary details

$12

$33

$75

How much do associate director clinical data management jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for associate director clinical data management in Michigan is $33.95, according to ZipRecruiter salary data. Most workers in this role earn between $25.58 and $33.94 per hour, depending on experience, location, and employer.

What is an associate director clinical data management?

An Associate Director of Clinical Data Management is a senior professional responsible for overseeing the planning, execution, and management of data collected in clinical trials within the pharmaceutical or biotechnology industry. They ensure that all clinical data is accurate, secure, and compliant with regulatory standards. This role typically involves leading teams, developing data management strategies, collaborating with cross-functional departments, and ensuring that projects are delivered on time and within budget. Associate Directors also play a key role in establishing best practices and continuous process improvements within the data management function.

What are the key skills and qualifications needed to thrive as an associate director clinical data management, and why are they important?

To thrive as an Associate Director Clinical Data Management, you need a strong background in clinical research, data management, and regulatory compliance, typically supported by a life sciences degree and several years of experience in clinical data management. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) platforms, and industry standards such as CDISC or GCP is crucial, with certifications like CCDM being advantageous. Leadership, strategic thinking, and excellent communication skills help drive cross-functional teams and ensure accurate data delivery. These competencies are vital because they ensure high-quality, compliant data management that supports successful clinical trials and regulatory submissions.

What is the difference between Associate Director Clinical Data Management vs Clinical Data Manager?

AspectAssociate Director Clinical Data ManagementClinical Data Manager
ResponsibilitiesOversees data management teams, develops strategies, ensures data quality and complianceManages data collection, validation, and database setup for clinical trials
Required CredentialsBachelor's/Master's in life sciences, experience in data management, leadership skillsBachelor's in life sciences, experience in clinical data handling, technical skills
Work EnvironmentSenior-level, strategic, often in larger organizations or departmentsOperational, hands-on, often in CROs or pharmaceutical companies

The Associate Director Clinical Data Management typically holds a higher strategic role, overseeing teams and ensuring data quality across projects, while the Clinical Data Manager focuses on day-to-day data handling tasks. Both roles require similar educational backgrounds and technical skills, but differ in scope and level of responsibility.

What are some common challenges faced by an associate director clinical data management, and how can they be addressed?

Associate Directors in Clinical Data Management often encounter challenges such as maintaining data quality across multiple studies, managing tight timelines, and ensuring compliance with evolving regulatory requirements. To address these, they implement robust data review processes, foster close collaboration between cross-functional teams (like biostatistics, clinical operations, and IT), and promote continuous training for their teams. Strong leadership and effective communication are key to navigating these challenges while delivering high-quality data for clinical trials.
What are popular job titles related to Associate Director Clinical Data Management jobs in Michigan? For Associate Director Clinical Data Management jobs in Michigan, the most frequently searched job titles are:
What job categories do people searching Associate Director Clinical Data Management jobs in Michigan look for? The top searched job categories for Associate Director Clinical Data Management jobs in Michigan are:
What cities in Michigan are hiring for Associate Director Clinical Data Management jobs? Cities in Michigan with the most Associate Director Clinical Data Management job openings:
Infographic showing various Associate Director Clinical Data Management job openings in Michigan as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 1% Temporary, and 4% Contract. Highlights an 91% Physical, 4% Hybrid, and 5% Remote job distribution, with an average salary of $70,617 per year, or $34 per hour.

Associate Director, External Data Acquisition and Delivery

Regeneron Pharmaceuticals

Warren, MI • Hybrid

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 10 days ago


Regeneron rating

8.7

Company rating: 8.7 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

14th of 86 rated pharmaceutical


Job description

Build our future together:

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director to join our Clinical Data Management team.

As an Associate Director, External Data Acquisition and Delivery (EDAD), you will provide strategic oversight and operational leadership for External Data Acquisition and Delivery activities across Regeneron's clinical trial portfolio and initiatives. You will ensure readiness of external data collection platforms, data conformance tools, reconciliation processes, and the delivery of high-quality, compliant external data from third-party vendors including laboratory, biomarker, Digital Health Technologies, imaging, ECG, PK, genomics, and specialty data. You will partner closely with Clinical Data Management, CROs, external vendors, and cross-functional partners to drive external data strategy, operational excellence, vendor oversight, digital transformation initiatives, and process improvements.

This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & where:

  • Work Location: Warren, NJ

  • Hybrid; 4 days per week on site

  • 25% Travel may be required

Discover your role:

  • Leading External Data Acquisition, integration, quality oversight, and delivery strategy across the clinical trial portfolio

  • Serving as a portfolio-level lead for external data quality and clinical-data operational strategy

  • Reviewing protocol requirements, vendor specifications, and operational data flows

  • Leading all aspects of development and maintenance of Data Transfer Specification (DTS) documents to ensure compliance with Regeneron standards and timelines

  • Providing expert mentorship on external data services including biomarker, eSource, eCOA, imaging, ECG, PK, genomics, and laboratory data

  • Driving external vendor oversight, onboarding, qualification, governance, and ongoing performance monitoring

  • Establishing and handling vendor KPIs, SLAs, and quality metrics

  • Governing reconciliation activities between EDC systems and vendor data platforms to ensure data integrity and consistency

  • Monitoring reconciliation metrics, discrepancy trends, and resolution timelines across studies

  • Collaborating with Database Development, Biostatistics, Study Data Managers, and external vendors to resolve complex data discrepancies

  • Leading process improvement initiatives, automation opportunities, and implementation of innovative external data solutions

  • Managing and developing a team of EDAD Managers, Specialists, and associates through coaching, mentoring, and performance management

  • Supporting SOP development, inspection readiness, audit activities, and regulatory compliance

  • Representing EDAD in leadership forums, governance committees, and technology discussions

This role requires:

  • Minimum 10+ years of experience in ClinicalDataAcquisition/Managementwithinbiotechnology, pharmaceutical, or healthcare industries

  • Minimum 4+ years of people management experience

  • Demonstrated experience overseeing external data reconciliation activities between EDC systems and vendor platforms

  • Experience driving process improvements and vendor oversight in supervised environments

  • Bachelor's degree in Science, Health, Mathematics, Computing, Information Systems, or a related field

  • Advanced degree preferred

  • Strong expertise managing multiple clinical external data types including biomarker, imaging, eCOA, ECG, PK, genomics, laboratory, and Digital Health Technology data

  • Advanced knowledge of external data reconciliation processes and EDC platforms such as Medidata Rave, Veeva, or Oracle Inform

  • Experience working with SAS, CSV, and XML data formats

  • Strong understanding of industry regulations including 21 CFR Part 11, ICH-GCP, and CDISC standards

  • Proven experience handling external vendor relationships and driving accountability for quality deliverables

  • Strong leadership, people management, coaching, and mentoring capabilities

  • Strategic thinking, creativity, problem-solving, and analytical skills

  • Strong project management and stakeholder management capabilities

  • Excellent verbal and written communication skills

  • Ability to work effectively in a fast-paced, matrixed, and global environment

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. 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, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.


Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed onsite. Please speak with your recruiter and hiring manager for more information about onsite expectations for your role and location.


As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.


For jobs in Canada: this posting is for an existing position.


Salary Range (annually)

$154,800.00 - $252,800.00

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