Senior Clinical Trial Associate – Clinical Ops

Aktis Oncology

. Support the planning, execution, and documentation of clinical trials involving radiopharmaceutical agents .

Posted 10/28/2026full-timeBoston • Massachusetts • United StatesSenior💰 $70,200 - $123,200 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial planning and execution, with strong knowledge of ICH-GCP guidelines and regulatory compliance. Proficient in project management and operational oversight, particularly in collaboration with CROs and vendors.

Highest-signal resume keywords

Clinical Research ExperienceICH-GCP Guidelines KnowledgeProject Planning/ManagementETMF/CTMS/EDC FamiliarityOncology Therapeutic Area Experience

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Clinical Trial DocumentationRegulatory Document ReviewMetrics TrackingQuality Control ChecksEnrollment Tracking

Soft Skills

Attention to DetailDecision-MakingCommunicationCollaborationAnalytic Skills

Tools & Technologies

ETMFCTMSEDC

Industry Keywords

Clinical TrialsPharmaceutical IndustryBiotech IndustryCRO IndustryPatient-Centric Approach

About the role

Key responsibilities & impact

Support the planning, execution, and documentation of clinical trials involving radiopharmaceutical agents
Support day-to-day operations of clinical trial conduct
Organize and maintain tracking systems and set up metrics and tools from study start-up to close-out
Track enrollment, monitoring visits, essential documents, and other study activities
Assist with development and review of protocols, ICFs, and clinical study plans
Schedule and coordinate study meetings, materials, and agendas
Record and disseminate study decisions and action items
Assist with creation, collection, and review of regulatory and study documents
Coordinate with CROs, vendors, and clinical sites
Compile study status reports and metrics for internal stakeholders
Perform ongoing quality-control checks of study documentation and eTMF
Assist in audit preparation and resolution of audit findings
Ensure inspection readiness
Report to the Senior Director, Clinical Operations and work under the direction of the Clinical Trial Manager or Clinical Operations Lead

Requirements

What you’ll need

Bachelor’s degree or equivalent, in life sciences, healthcare, or related field
Minimum of 1-3 years of clinical research experience, preferably in the pharmaceutical, biotech and/or CRO industry
Oncology therapeutic area experience is preferred
Strong knowledge of ICH-GCP guidelines and Code of Federal Regulations
Clinical research operational knowledge and computer literacy
Strong project planning/management, including oversight of CROs/vendors
Experience interacting with global or regional teams in a virtual environment
Familiarity with clinical trial systems such as eTMF, CTMS, or EDC is a plus
Strong attention to detail, decision-making, communication/collaboration, and analytic skills
Ability to seek solutions to issues
Willingness to travel up to 10-20% of time
Strong desire to be part of a patient-centric company
Proven transparent communication and ability to foster open and diverse debate
Ability to work with agility and manage ambiguity

Benefits

Comp & perks

Equal Opportunity Employer commitment
Work environment free from unlawful harassment, discrimination, or retaliation
Willingness to travel up to 10-20% of time for site visits, conferences, etc. (role-related allowance)