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Associate, Clinical Operations (RID00214)

Role overview

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

Responsibilities

  • 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

Key facts

Hard skills

Other skills

  • Microsoft Office
  • Communication
  • Teamwork

About the company

Red Nucleus logo

Red Nucleus

Contract Research Organizations (CRO)

We are a global strategic partner with decades of experience across the entire life sciences product lifecycle. We excel in providing our clients with unique insights and efficiencies to support them in their journey to improve health outcomes and ultimately the quality of people’s lives. By connecting our full suite of products and services from scientific and advisory services, market access, medical communications and learning and development, we are the “red thread” to lead our life sciences clients through transformational change to accelerate customer success. Visit the new rednucleus.com to learn more.

Company details

Company typeSME
IndustryContract Research Organizations (CRO)
Company size501 - 1000

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Job description

Associate / Senior Associate, Clinical Operations

Clinical Research | SS&A

Do you enjoy managing complex clinical studies while helping bring innovative research technologies to patients and sites?


We're seeking an Associate / Senior 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: 1-10 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

  • Digital health or mobile application experience
  • Experience in rare diseases, gene therapy, or long-term follow-up studies
  • Knowledge of clinical drug development pathways, including Phase I-III studies and registries

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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Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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