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 ...
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 ...
Unblinded Clinical Research Coordinator II (4021)
Southfield, MI · On-site
$22.25 - $29.50/hr
Perform regular audits on the clinical data to assess percent completeness and accuracy * Assist in ... Associates Degree required or 2 years of formal educational coursework * Bachelor's degree ...
Unblinded Clinical Research Coordinator II (4021)
Southfield, MI · On-site
$22.25 - $29.50/hr
Perform regular audits on the clinical data to assess percent completeness and accuracy * Assist in ... Associates Degree required or 2 years of formal educational coursework * Bachelor's degree ...
Unblinded Clinical Research Coordinator II (4021)
Southfield, MI · On-site
$22.25 - $29.50/hr
Perform regular audits on the clinical data to assess percent completeness and accuracy * Assist in ... Associates Degree required or 2 years of formal educational coursework * Bachelor's degree ...
Unblinded Clinical Research Coordinator II (4021)
Southfield, MI · On-site
$22.25 - $29.50/hr
Perform regular audits on the clinical data to assess percent completeness and accuracy * Assist in ... Associates Degree required or 2 years of formal educational coursework * Bachelor's degree ...
Clinical Research Associate II/Sr. CRA
Detroit, MI · On-site +1
Performing data review and resolution of queries to maintain high-quality clinical data ... Minimum of 2 years of experience as a Clinical Research Associate. * In-depth knowledge of clinical ...
Clinical Research Associate II/Sr. CRA
Detroit, MI · On-site +1
Performing data review and resolution of queries to maintain high-quality clinical data ... Minimum of 2 years of experience as a Clinical Research Associate. * In-depth knowledge of clinical ...
Performing data review and resolution of queries to maintain high-quality clinical data ... Minimum of 2 years of experience as a Clinical Research Associate. * In-depth knowledge of clinical ...
Performing data review and resolution of queries to maintain high-quality clinical data ... Minimum of 2 years of experience as a Clinical Research Associate. * In-depth knowledge of clinical ...
Performing data review and resolution of queries to maintain high-quality clinical data ... Minimum of 2 years of experience as a Clinical Research Associate. * In-depth knowledge of clinical ...
Quick apply
Performing data review and resolution of queries to maintain high-quality clinical data ... Minimum of 2 years of experience as a Clinical Research Associate. * In-depth knowledge of clinical ...
Clinical Documentation Specialist I FT Days
$34.50 - $46.25/hr
Compiles, analyzes and evaluates quality and clinical data collected as part of an integrated ... OR Associate's degree in applied sciences or related field with emphasis in healthcare. * Bachelors ...
Clinical Documentation Specialist I FT Days
$34.50 - $46.25/hr
Compiles, analyzes and evaluates quality and clinical data collected as part of an integrated ... OR Associate's degree in applied sciences or related field with emphasis in healthcare. * Bachelors ...
Senior Manager Data Lead
Detroit, MI · Hybrid
Healthcare Provider L65 - Associate Vice President, AI and Data Solutions - Data Lead Join our AI ... Clinical data exchange and coding standards, including HL7, FHIR, and ICD * Data operations (ie ...
Senior Manager Data Lead
Detroit, MI · Hybrid
Healthcare Provider L65 - Associate Vice President, AI and Data Solutions - Data Lead Join our AI ... Clinical data exchange and coding standards, including HL7, FHIR, and ICD * Data operations (ie ...
Research Abstract Analyst III- Full time- Central Abstractor Office- One Ford Place
Detroit, MI · On-site
Abstracts clinical data to satisfy numerous HFHS/HAP compliance and quality initiatives: COE's, P4P ... Associate degree Health Information Management or related field, in addition to maintaining one of ...
Research Abstract Analyst III- Full time- Central Abstractor Office- One Ford Place
Detroit, MI · On-site
Abstracts clinical data to satisfy numerous HFHS/HAP compliance and quality initiatives: COE's, P4P ... Associate degree Health Information Management or related field, in addition to maintaining one of ...
Research Abstract Analyst III- Full time- Central Abstractor Office- One Ford Place
Detroit, MI · On-site
Abstracts clinical data to satisfy numerous HFHS/HAP compliance and quality initiatives: COE's, P4P ... Associate degree Health Information Management or related field, in addition to maintaining one of ...
Research Abstract Analyst III- Full time- Central Abstractor Office- One Ford Place
Detroit, MI · On-site
Abstracts clinical data to satisfy numerous HFHS/HAP compliance and quality initiatives: COE's, P4P ... Associate degree Health Information Management or related field, in addition to maintaining one of ...
Translate emerging biomarker and mechanism-of-action data into diagnostic target product profiles ... Lead analytical and clinical validation planning (accuracy, precision, sensitivity/specificity ...
Translate emerging biomarker and mechanism-of-action data into diagnostic target product profiles ... Lead analytical and clinical validation planning (accuracy, precision, sensitivity/specificity ...
Senior Pharmacovigilance System Architect (Argus Administrator) - US
Canton, MI · On-site
$120 - $180/hr
Provides technical assistance and support to Drug Safety Associate team with electronic submissions ... Strong understanding of global clinical trial development and data. Requirements * College graduate ...
Senior Pharmacovigilance System Architect (Argus Administrator) - US
Canton, MI · On-site
$120 - $180/hr
Provides technical assistance and support to Drug Safety Associate team with electronic submissions ... Strong understanding of global clinical trial development and data. Requirements * College graduate ...
In this role, you will support the Clinical Study Lead by taking responsibility for areas of ... Supports data quality including regular review of data metrics and listings, protocol deviations ...
In this role, you will support the Clinical Study Lead by taking responsibility for areas of ... Supports data quality including regular review of data metrics and listings, protocol deviations ...
In this role, you will support the Clinical Study Lead by taking responsibility for areas of ... Supports data quality including regular review of data metrics and listings, protocol deviations ...
In this role, you will support the Clinical Study Lead by taking responsibility for areas of ... Supports data quality including regular review of data metrics and listings, protocol deviations ...
In this role, you will support the Clinical Study Lead by taking responsibility for areas of ... Supports data quality including regular review of data metrics and listings, protocol deviations ...
In this role, you will support the Clinical Study Lead by taking responsibility for areas of ... Supports data quality including regular review of data metrics and listings, protocol deviations ...
Medical record and research source documentation verification against case report form data ... Clinical Research Associate Experience (minimum 1 year), hematology/oncology exerience preferred
Medical record and research source documentation verification against case report form data ... Clinical Research Associate Experience (minimum 1 year), hematology/oncology exerience preferred
Basic proficiency in computer use (Windows/PC) and data entry * Ability to learn and achieve ... Job Detail Job Opening ID 278571 Working Title Clinical Quality Support Associate Job Title OFFICE ...
Basic proficiency in computer use (Windows/PC) and data entry * Ability to learn and achieve ... Job Detail Job Opening ID 278571 Working Title Clinical Quality Support Associate Job Title OFFICE ...
Clinical Research Coord Assoc
Brighton, MI · On-site
$23.25 - $31/hr
Data Management and Informatics * Leadership and Professionalism * Communication and Teamwork Due ... Clinical Research Coordinator - Associate * Demonstrates understanding of protocol elements ...
Clinical Research Coord Assoc
Brighton, MI · On-site
$23.25 - $31/hr
Data Management and Informatics * Leadership and Professionalism * Communication and Teamwork Due ... Clinical Research Coordinator - Associate * Demonstrates understanding of protocol elements ...
Associate Director Pharmacometrics Programming provides timely support to the study team on all ... Lead programming support for processing/analyzing/storing data from clinical studies according to a ...
Associate Director Pharmacometrics Programming provides timely support to the study team on all ... Lead programming support for processing/analyzing/storing data from clinical studies according to a ...
MMS is an award-winning, data-focused clinical research organization (CRO). We pride ourselves on ... Provides technical assistance and support to Drug Safety Associate team with electronic submissions ...
Quick apply
MMS is an award-winning, data-focused clinical research organization (CRO). We pride ourselves on ... Provides technical assistance and support to Drug Safety Associate team with electronic submissions ...
Clinical Data Associate information
See Canton, MI salary details
$12.92 - $19.06
5% of jobs
$19.06 - $25.19
6% of jobs
$27.56 is the 25th percentile. Wages below this are outliers.
$25.19 - $31.33
35% of jobs
The median wage is $31.93 / hr.
$31.33 - $37.47
38% of jobs
$37.47 - $43.60
6% of jobs
$43.60 - $49.74
3% of jobs
$49.74 - $55.88
2% of jobs
$55.88 - $62.01
0% of jobs
$62.01 - $68.15
0% of jobs
$68.15 - $74.29
1% of jobs
$74.29 - $80.42
3% of jobs
$12
$36
$80
How much do clinical data associate jobs pay per hour?
What does a clinical data associate do?
What does a clinical data associate do?
A clinical data associate is responsible for tracking data and results in a research study. As a clinical data associate, your job duties are to collect data, perform data management, and input data into any software used by your team. You work on a research team, so you must be able to work collaboratively and have excellent organizational skills. While you spend most of your time in an office, you may be required to work in the field to record data. The only universal qualifications needed for this career are a background in health care or medical science research and experience with data management software like Oracle Clinical, Microsoft Excel, and SPSS.
What are the key skills and qualifications needed to thrive as a clinical data associate, and why are they important?
What are some common challenges faced by clinical data associates when ensuring data quality during clinical trials?
What is the difference between Clinical Data Associate vs Clinical Research Coordinator?
| Aspect | Clinical Data Associate | Clinical Research Coordinator |
|---|---|---|
| Primary Role | Manage and ensure accuracy of clinical trial data | Oversee trial operations, patient recruitment, and site management |
| Credentials | Bachelor's in life sciences or related field; familiarity with data management | Bachelor's in health sciences or related field; clinical trial experience |
| Work Environment | Data management teams, clinical trial databases | Clinical sites, hospitals, research facilities |
| Industry Usage | Pharmaceutical companies, CROs, biotech firms | Hospitals, research institutions, clinical trial sites |
While both roles support clinical trials, a Clinical Data Associate primarily focuses on managing and validating trial data, ensuring accuracy and compliance. In contrast, a Clinical Research Coordinator handles the overall trial operations, including patient recruitment and site coordination. Both roles require relevant certifications and work within the clinical research industry, but their daily responsibilities differ significantly.
What are the most commonly searched types of Clinical Data jobs in Canton, MI?
The most popular types of Clinical Data jobs in Canton, MI are:
What are popular job titles related to Clinical Data Associate jobs in Canton, MI?
For Clinical Data Associate jobs in Canton, MI, the most frequently searched job titles are:
What job categories do people searching Clinical Data Associate jobs in Canton, MI look for?
The top searched job categories for Clinical Data Associate jobs in Canton, MI are:
What cities near Canton, MI are hiring for Clinical Data Associate jobs?
Cities near Canton, MI with the most Clinical Data Associate job openings:

Associate Director, External Data Acquisition and Delivery
Warren, MI • Hybrid
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Re-posted 21 days ago
Regeneron rating
8.4
Based on 43 frontline employees who took The Breakroom Quiz
22nd 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 - $252,800.00What Regeneron employees say
Pay
Benefits
Hours and flexibility
Workplace
Get the full story on Breakroom
About Regeneron
Sourced by ZipRecruiter
Industry
Biotechnology research and development
Company size
5,001 - 10,000 Employees
Headquarters location
Tarrytown, NY, US
Year founded
1988