Source Job

  • Lead and manage a team of 15-17 Study Management Associates to ensure best-in-class study execution.
  • Drive performance management, development, and training of direct reports in a global, remote team environment.
  • Support resource planning and process improvements to meet organizational goals and business continuity.

People Management Clinical Research Mentoring Strategic Planning

20 jobs similar to Study Management Associate

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$96,500–$183,500/yr
Global

  • Leads and oversees global clinical trials from inception through closure, ensuring quality and efficiency.
  • Manages external vendors, recruitment strategies, and cross-functional team coordination.
  • Maintains inspection readiness and contributes to risk management and process improvement.

AbbVie discovers and delivers innovative medicines and solutions for serious health issues across immunology, oncology, and neuroscience. The company is a global biopharmaceutical leader with a focus on making a remarkable impact.

US

  • Manage end-to-end clinical studies ensuring on-time and on-budget delivery with high quality standards.
  • Lead multifunctional study management teams and serve as primary point of contact for client study teams.
  • Oversee project planning, resource allocation, and financial management while ensuring regulatory compliance.

Science 37 is a clinical research organization focused on decentralized clinical trials. They value employee well-being and provide an equal opportunity workplace.

Global

  • Lead and oversee global clinical trials from inception to closure, managing cross-functional teams and vendors.
  • Ensure compliance with ICH/GCP and regulatory standards while driving recruitment and risk management strategies.
  • Manage study materials, systems (EDC, IRT, CTMS), and provide training to stakeholders.

AbbVie is a biopharmaceutical company focused on discovering and delivering innovative medicines in immunology, oncology, neuroscience, and aesthetics. With a global presence, they emphasize integrity, innovation, and community service.

Spain

  • Responsible for executing one or more elements of clinical studies in compliance with quality standards and regulations.
  • Supports the Study Project Manager in leading cross-functional study teams and developing study protocols.
  • Manages vendor selection, oversight, and study-related training, and proactively resolves issues.

AbbVie is a biopharmaceutical company focused on discovering and delivering innovative medicines and solutions for serious health issues. It is a large global organization with a diverse workforce and a commitment to integrity and innovation.

United States

  • Lead, mentor, and coach a team of over 50 direct and indirect reports to foster a high-performance culture.
  • Oversee daily Patient Service Center operations to ensure efficient, compliant, and high-quality service delivery.
  • Analyze KPIs, customer feedback, and operational data to drive continuous improvement and enhance patient and provider experiences.

The company provides patient support program services in the healthcare industry. The culture emphasizes operational excellence, compliance, and patient-centered care, with a large team environment.

US

  • Collaborate with project teams and clinical sites to support study startup, training, and device deployment.
  • Ensure compliance with GCP, ICH guidelines, and regulatory standards while monitoring project progress.
  • Address operational issues and provide feedback to improve devices and workflows.

Beacon Biosignals is transforming precision medicine for the brain by offering at-home EEG platforms for clinical development and diagnostics. The company fosters a remote-first culture with office hubs in Boston, New York, and Paris, emphasizing asynchronous work and collaboration.

$135,000–$159,000/yr
US

  • Provide study oversight as the primary liaison between CRAs, site staff, clients, and vendors across all study stages.
  • Ensure clinical monitoring activities comply with SOPs, regulations, GCPs, and study-specific requirements.
  • Support team training, review site visit reports, and manage oversight of the Trial Master File and eTMF.

ProTrials is a women-owned, WBENC-certified Contract Research Organization (CRO) trusted since 1996, delivering ethical services to pharmaceutical, biotech, and medical device companies. They foster a collaborative community where team members feel valued and empowered to make a meaningful impact on global health.

$90,000–$110,000/yr
US

  • Oversee clinical study operations from startup through close-out, ensuring quality and compliance.
  • Act as primary operational partner to sponsors, project teams, and clinical sites.
  • Foster a culture of quality by coaching peers on GCP compliance and documentation discipline.

Beacon Biosignals is transforming precision medicine for the brain, offering EEG and cardiopulmonary platforms for clinical development and diagnostics. The company has office hubs in Boston, New York, and Paris, and fosters a first-class remote work culture with a focus on diversity and impact.

$165,000–$180,000/yr
US 4w PTO

  • Lead clinical trial execution and operational delivery across internal and external stakeholders from start-up through execution.
  • Provide oversight of CROs, vendors, and clinical trial partners to ensure quality, compliance, timelines, and budget objectives are achieved.
  • Serve as the Clinical Operations leader for the team of CTMs, CRAs, and CTAs for each assigned project.

Immatics is a global leader in precision targeting of PRAME for cancer immunotherapy, with a robust clinical pipeline spanning TCR T-cell therapies and TCR bispecifics. The company fosters a collaborative and innovative culture focused on making a meaningful impact on patients.

US

  • Independently manages significant aspects of clinical trials and research projects.
  • Trains and provides guidance to less experienced staff, and oversees data management.
  • Ensures compliance with regulations, monitors IRB submissions, and interfaces with study sponsors.

Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate and prepare leaders for the future. The university is committed to diversity and inclusion, providing a supportive environment for staff and faculty.

UK Spain Poland Hungary Romania Serbia Slovakia

  • Serve as primary point-of-contact liaison with clients, providing outstanding customer service and participating in proposal activities and client presentations.
  • Oversee all aspects of clinical research trials, directing project managers and ensuring consistency across assigned portfolios.
  • Manage study budgets, financial health, and project plans, including risk management and quality assurance, while leading cross-functional teams.

Precision Medicine Group is a people-focused CRO that combines novel clinical trial designs, industry-leading operational and medical authorities, and advanced biomarker and data analytics solutions, with a passion for rare diseases and oncology. The company fosters a supportive and collaborative environment, promoting work-life balance and team development, with a growing team dedicated to ground-breaking cancer therapies.

Europe

  • We oversee a team of Clinical Research Project Managers delivering clinical studies and observational research programs.
  • We shape team performance, resource strategy, operational excellence, and talent development across a diverse project portfolio.
  • We ensure delivery against scope, timelines, budgets, quality standards, client expectations, and business objectives.

Jobgether uses AI-powered matching to connect candidates with hiring companies. This position is listed on behalf of a partner company that manages all applications, and the role is within a clinical research organization focused on delivering clinical studies and observational research programs.

  • Lead a team of Nurse Educators and Non-Clinical Support to provide world-class patient outreach experiences.
  • Manage client relationships and ensure compliance with operational practices and quality standards.
  • Coach and mentor team members to improve confidence, product knowledge, and communication skills.

Momentum Life Sciences partners with life science companies to design and deliver patient support programs that drive better health outcomes. With over 30 years of experience in the healthcare industry, they foster a collaborative and empowering culture.

$161,800–$199,800/yr
United States

  • Manage day-to-day clinical trial operations, including CRO/vendor oversight and site management.
  • Lead cross-functional study teams, develop study documents, and implement risk mitigation strategies.
  • Ensure high-quality deliverables within timelines and budget, from start-up through close-out.

Ultragenyx is a biopharmaceutical company dedicated to developing life-changing treatments for rare diseases. They foster a supportive and inclusive culture focused on learning and growth, with a global team committed to innovation.

US Unlimited PTO

  • Manage clinical study vendors and ensure deliverables are on time, within budget, and compliant with FDA and ICH/GCP guidelines.
  • Support CRO collaboration, site start-up, study documentation, and risk mitigation with cross-functional teams.
  • Leverage AI tools and process improvements to enhance clinical operations productivity and quality.

This biotechnology company focuses on developing innovative oncology therapies. It offers a collaborative, multidisciplinary environment with opportunities to use AI-enabled tools and modern approaches to clinical operations.

US

  • Serve as the primary point of contact for assigned protocols, linking Country Operations with the clinical trial team.
  • Manage project timelines, deliverables, and performance for clinical studies from feasibility to close out.
  • Ensure compliance with ICH/GCP, country regulations, and company policies while leading local study teams.

Merck is a global healthcare leader with a diverse range of prescription medicines, vaccines, and animal health products. With over 100 years of history, the company employs tens of thousands worldwide and fosters a culture of innovation and inclusivity.

$95,000–$125,000/yr
US Unlimited PTO

  • Oversee study start-up, site activation, and close-out activities while managing study plans and essential documents.
  • Collaborate with cross-functional teams, sponsors, and vendors to ensure timely and compliant project execution.
  • Mentor CTA team members and contribute to TMF quality, inspection readiness, and regulatory compliance.

ProTrials is a women-owned, WBENC-certified Contract Research Organization (CRO) that has been a trusted partner in clinical research since 1996. They are a collaborative community committed to making a meaningful impact on global health, valuing team members and empowering them.

India Unlimited PTO 12w maternity 12w paternity

  • Lead a team of Research Advisors, ensuring high utilization and delivering exceptional client service.
  • Manage and mentor team members on project delivery, retention, and growth.
  • Track team metrics like utilization and CSAT, and participate in hiring interviews.

Dscout builds a flexible UX research platform trusted by top brands in finance, healthcare, consumer goods, and tech to understand users deeply. They are a recognized leader with a diverse, inclusive team that prioritizes learning and sharing.

  • Lead cross-functional trial teams to execute global clinical trials from start-up to closeout.
  • Oversee CRO/vendor selection, budget management, and operational risk mitigation.
  • Ensure compliance with regulations and GCP, and foster team development and mentorship.

Alnylam Pharmaceuticals is a biopharmaceutical company that translates RNA interference (RNAi) into a new class of innovative medicines for rare and prevalent diseases. With a people-first culture and core values of innovation and excellence, Alnylam is a top employer recognized globally.

$250,000–$270,000/yr
US Unlimited PTO 16w maternity 8w paternity

  • Owns the people-management engine behind the care team, ensuring hiring, training, and performance drive predictable outcomes.
  • Develops demand-per-member models that accurately allocate care team resources based on member complexity.
  • Designs and governs SOPs, SLAs, and algorithms that operationalize care team workflows system-wide.

Twin Health empowers people to improve and prevent chronic metabolic diseases like type 2 diabetes and obesity using AI Digital Twin technology. With over $100 million in funding, Twin is scaling rapidly across the US and globally, recognized as an innovator and top workplace.