Associate, Clinical Data Management (RID00216)
Posted 7 days agoConfirmed open 27 min ago
Who can apply
United States only
Salary
Not disclosed
Level
Entry level
Full-time
Timezone
Not stated
About the role
Associate / Senior Associate, Clinical Data Management
Clinical Research | Red Nucleus
Are you passionate about clinical data quality and the future of patient-centered research?
We're looking for an Associate / Senior Associate, Clinical Data Management to support the delivery and oversight of clinical and patient-reported data within EDC platforms, including our innovative iTakeControl (iTC) technology. You'll work across clinical operations, product, and technical teams while supporting studies from startup through closeout.
Experience Level: 0-10 years
Required Qualifications
- Undergraduate degree or equivalent professional experience
- Experience supporting clinical study protocols, protocol amendments, observational research, registries, data migrations, reporting, and data transfers
- Professional experience within biopharma, pharmaceutical, CRO, clinical site, or consulting environments
- Knowledge of GCP, ICH, HIPAA, GDPR, FDA requirements, FDA 21 CFR Part 11, Annex 11, and GxP processes
- Experience with or understanding of EDC, ePRO, EHR, clinical research technologies, and health data collection systems
- Experience managing multiple projects, timelines, stakeholders, vendors, and study teams simultaneously
- Strong written and verbal communication skills with proficiency in Microsoft Office (Word, Excel, PowerPoint)
What You'll Do
- Manage and review clinical and ePRO data, including video-based data collection
- Develop Data Management Plans, CRF Specifications, eCRFs, and study documentation
- Support data transfers, exports, migrations, and reconciliation activities
- Participate in site initiation visits, user acceptance testing (UAT), and product launches
- Collaborate with sponsors, sites, vendors, and cross-functional teams
- Support innovative approaches to remote data monitoring and patient-centric research
Nice to Have
- Digital health, digital therapeutics, or mobile application experience
- Experience in rare diseases, gene therapy, or long-term follow-up studies
- Experience working with central or specialty laboratories/vendors
- Familiarity with CDISC, CDASH, SDTM, FHIR, OMOP, MedDRA, and WHO Drug standards and dictionaries
Diversity, equity and inclusion are valued at Red Nucleus and we believe we have a shared responsibility to provide equal opportunity and foster an inclusive spirit. We do not discriminate on the basis of race, color, national origin, religion, caste, sexual orientation, gender, age, marital status, veteran status, or disability status.
To learn more about working at Red Nucleus, please visit Careers | Red Nucleus.
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About Red Nucleus
Listing details & historyShowHide
- Employer posted
- 22 Oct 2026
- Last confirmed open
- 27 min ago
- Source
- Employer careers site
- Degree
- Degree or equivalent experience
- “Experience Level: 0-10 years Required Qualifications Undergraduate degree or equivalent professional experience Experience supporting clinical study protocols, protocol amendments, observational research, registries, data migrations, reporting, and data transfers Professional experience within biopharma, pharmaceutical, CRO, clinical site, or consu”
- Visa
- Not stated
- “Experience Level: 0-10 years Required Qualifications Undergraduate degree or equivalent professional experience Experience supporting clinical study protocols, protocol amendments, observational research, registries, data migrations, reporting, and data transfers Professional experience within biopharma, pharmaceutical, CRO, clinical site, or consulting environments Knowledge of GCP, ICH, HIPAA, GDPR, FDA requirements, FDA 21 CFR Part 11, Annex 11, and GxP processes Experience with or understanding of EDC, ePRO, EHR, clinical research technologies, and health data collection systems Experience managing multiple projects, timelines, stakeholders, vendors, and study teams simultaneously Strong written and verbal communication skills with proficiency in Microsoft Office (Word, Excel, PowerPoint) What You'll Do Manage and review clinical and ePRO data, including video-based data collection Develop Data Management Plans, CRF Specifications, eCRFs, and study documentation Support data transfers, exports, migrations, and reconciliation activities Participate in site initiation visits, user acceptance testing (UAT), and product launches Collaborate with sponsors, sites, vendors, and cross-functional teams Support innovative approaches to remote data monitoring and patient-centric research Nice to Have Digital health, digital therapeutics, or mobile application experience Experience in rare diseases, gene therapy, or long-term follow-up studies Experience working with central or specialty laboratories/vendors Familiarity with CDISC, CDASH, SDTM, FHIR, OMOP, MedDRA, and WHO Drug standards and dictionaries Diversity, equity and inclusion are valued at Red Nucleus and we believe we have a shared responsibility to provide equal opportunity and foster an inclusive spirit.”
- Timezone
- Not stated
- Languages
- Not stated
- Location evidence
- “Remote (Yardley, Pennsylvania, United States)”
Details are read from the listing text. They are not a guarantee of work authorization; confirm with the employer.
