Graduate Clinical Research Associate, CRA

Invences Consulting

. Participate fully in the 8-week CRA Training Program, including structured learning, functional rotations, and assessments .

Posted 11/3/2026full-timeUnited StatesEntry Level💰 $60,000 - $65,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial support, including site management, documentation, and adherence to regulatory standards such as ICH GCP. Proficient in maintaining clinical trial systems and providing effective communication and collaboration within clinical teams.

Highest-signal resume keywords

Clinical Trial SupportSite Management ActivitiesICH GCP ComplianceData Review and Query ResolutionOrganizational and Time Management Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical ResearchTrial Master File CoordinationDocument FilingQuality ChecksClinical Trial Management Systems (CTMS)Electronic Trial Master File (eTMF)Electronic Case Report Form (eCRF)Study AdministrationRegulatory ComplianceSafety Monitoring

Soft Skills

Learning AgilityAttention to DetailTeam CollaborationEffective CommunicationOrganizational Skills

Industry Keywords

Clinical Research CoordinatorClinical Trial AssistantClinical Trial AdministratorOncologyImmunologyCNSClinical SOPsStudy Close-Out SupportInvestigator Site FilesProfessional Communication

About the role

Key responsibilities & impact

Participate fully in the 8-week CRA Training Program, including structured learning, functional rotations, and assessments
Participate in coaching and mentoring with Line Managers, cross-functional stakeholders, the assigned Senior CRA mentor, and graduate cohort peers
Support supervised site management activities, including maintaining essential site documentation and Investigator Site Files
Assist with Trial Master File coordination, document filing, quality checks, and completeness
Support preparation for monitoring visits, participate in co-monitoring or observational visits, and complete routine follow-up activities under guidance
Support data review, query resolution, and maintenance of clinical trial systems such as CTMS, eTMF, and eCRF
Provide in-house support to clinical trial teams, internal teams, sites, and vendors on assigned studies
Assist with study administration, including basic finance, regulatory, safety, and study close-out support
Apply Novotech quality standards, ICH GCP, and regulatory requirements; promptly escalate risks, issues, and safety concerns
Adhere to company processes and assist in reviewing and developing clinical SOPs and processes
Maintain professional internal and external communications reflecting Novotech’s company image
Progress toward CRA I and subsequently CRA II subject to performance, readiness, and successful training completion

Requirements

What you’ll need

Completed Bachelor's degree in clinical research or a life sciences-related field
Prior experience as a Clinical Research Coordinator, Clinical Trial Assistant, or Clinical Trial Administrator with therapeutic specialization in oncology, immunology, and CNS preferred
Strong learning agility
Attention to detail
Organizational and time management skills
Ability to work effectively in a team
Confidence using computer-based systems
Ability and willingness to travel 8–10 DOS after completion of the training program
Visa sponsorship/authorization is not supported for this role

Benefits

Comp & perks

Flexible working options
Paid parental leave for both parents
Flexible leave entitlements
Wellness programs
Ongoing development programs
Salary increase upon successful completion of the training program