Associate, Clinical Operations (RID00214)
Posted 7 days agoConfirmed open 1h ago
Who can apply
United States only
Salary
Not disclosed
Level
Entry level
Full-time
Timezone
Not stated
About the role
Associate, Clinical Operations
Clinical Research | Red Nucleus
Do you enjoy managing complex clinical studies while helping bring innovative research technologies to patients and sites?
We're seeking an Associate, Clinical Operations to support clinical research studies, including programs utilizing remote data capture technologies such as video assessments, ePRO, and eCOA solutions.
Experience Level: 0-5 years
Required Qualifications
- Undergraduate degree or equivalent professional experience
- Experience operationalizing clinical study protocols, amendments, observational research studies, and registries
- Professional experience within biotech, pharmaceutical, CRO, clinical site, or consulting environments
- Knowledge of GCP, ICH, HIPAA, GDPR, FDA requirements, and clinical research regulations
- Experience managing multiple research projects, vendors, sponsors, sites, and stakeholders simultaneously
- Working knowledge of EDC, ePRO, EHR, and clinical research technologies
- Strong written and verbal communication skills and proficiency with Microsoft Office (Word, Excel, PowerPoint)
What You'll Do
- Support studies from startup through closeout
- Manage sponsor, site, and vendor relationships
- Participate in protocol design discussions and implementation planning
- Develop IRB submission packages, training materials, caregiver/site manuals, and operational documentation
- Lead or support Site Initiation Visits (SIVs), site training, and central rater training
- Partner with Data Management, Product Management, and Technical Delivery teams
- Support UAT and product launches
Nice to Have
- 0-5 years of experience in clinical research, project management, or related life sciences settings
- Experience supporting rare disease, gene therapy, or long-term follow-up research programs
- Experience working with sponsors, CROs, and external vendors
- Exposure to digital health, mobile applications, or technology-enabled clinical research solutions
- Understanding of clinical drug development, including Phase I-III clinical trials, registries, and observational studies
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Strong problem-solving, communication, and collaboration skills, with the ability to work effectively in a team-based environment
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
- 1h ago
- Source
- Employer careers site
- Degree
- Degree or equivalent experience
- “Experience Level: 0-5 years Required Qualifications Undergraduate degree or equivalent professional experience Experience operationalizing clinical study protocols, amendments, observational research studies, and registries Professional experience within biotech, pharmaceutical, CRO, clinical site, or consulting environments Knowledge of GCP, ICH, ”
- Visa
- Not stated
- “Experience Level: 0-5 years Required Qualifications Undergraduate degree or equivalent professional experience Experience operationalizing clinical study protocols, amendments, observational research studies, and registries Professional experience within biotech, pharmaceutical, CRO, clinical site, or consulting environments Knowledge of GCP, ICH, HIPAA, GDPR, FDA requirements, and clinical research regulations Experience managing multiple research projects, vendors, sponsors, sites, and stakeholders simultaneously Working knowledge of EDC, ePRO, EHR, and clinical research technologies Strong written and verbal communication skills and proficiency with Microsoft Office (Word, Excel, PowerPoint) What You'll Do Support studies from startup through closeout Manage sponsor, site, and vendor relationships Participate in protocol design discussions and implementation planning Develop IRB submission packages, training materials, caregiver/site manuals, and operational documentation Lead or support Site Initiation Visits (SIVs), site training, and central rater training Partner with Data Management, Product Management, and Technical Delivery teams Support UAT and product launches Nice to Have 0-5 years of experience in clinical research, project management, or related life sciences settings Experience supporting rare disease, gene therapy, or long-term follow-up research programs Experience working with sponsors, CROs, and external vendors Exposure to digital health, mobile applications, or technology-enabled clinical research solutions Understanding of clinical drug development, including Phase I-III clinical trials, registries, and observational studies Strong problem-solving, communication, and collaboration skills, with the ability to work effectively in a team-based environment 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.
