Local Study Associate Director - Oncology [Remote]
jobgether
- Remote job
This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Local Study Associate Director - Oncology based in the United States.
This role sits at the heart of clinical study delivery within a country environment, driving end-to-end execution of oncology trials.
It combines strategic oversight with hands-on operational leadership across local study teams.
You will ensure studies are delivered on time, within budget, and in full compliance with regulatory and quality standards.
The position plays a key role in strengthening site performance, patient recruitment, and data quality.
You will collaborate closely with global stakeholders, investigators, and cross-functional partners.
This is a high-impact role in a fast-paced clinical research setting where precision, leadership, and adaptability are essential.
It offers the opportunity to directly contribute to the advancement of innovative oncology therapies for patients.
Accountabilities:
- Lead and coordinate Local Study Teams (CRAs, CSAs) to ensure successful delivery of oncology clinical trials at country level.
- Oversee all trial and site activities including feasibility, site selection, activation, monitoring, close-out, and documentation archiving.
- Ensure compliance with ICH-GCP, local regulations, and applicable procedural requirements throughout study execution.
- Drive patient recruitment strategies and maintain strong communication with investigators and site staff.
- Manage risk identification and mitigation plans while proactively resolving operational issues.
- Supervise study progress reporting, resource planning, budgeting, and vendor/stakeholder coordination.
- Support audits, inspections, and maintain inspection-ready trial documentation (including eTMF).
- Contribute to continuous process improvement and mentor junior team members.
Requirements:
- Minimum 3+ years of experience in clinical development operations managing end-to-end trials within CRO or pharmaceutical environments, ideally in the US.
- Proven experience in oncology clinical trial management.
- Strong knowledge of ICH-GCP guidelines and applicable local regulatory frameworks.
- Demonstrated leadership ability in managing cross-functional teams and complex clinical projects.
- Excellent project management, organizational, and prioritization skills.
- Strong communication, interpersonal, and stakeholder management abilities.
- High attention to detail with the ability to manage multiple priorities in a fast-paced environment.
- Fluency in English required; additional local language proficiency is a plus.
- Bachelor’s degree in life sciences or a related field (or equivalent qualification).
- Ability to travel nationally and internationally as required.
- Strong ethical standards, adaptability, and proficiency with clinical IT systems.
Benefits:
- Competitive compensation aligned with experience and industry standards.
- Comprehensive health, dental, and vision insurance coverage.
- Opportunities for career development within global clinical research programs.
- Flexible work arrangements depending on project and business needs.
- Exposure to global oncology studies and cutting-edge clinical development programs.
- Supportive, collaborative, and multicultural working environment.
- Access to continuous learning, training, and professional development resources.
How Jobgether works:
We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team.
We appreciate your interest and wish you the best!
Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time.
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We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
$137.94k - $206.91k
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