Source Job

US

  • Designs and aligns operational plans to study and company objectives; balances short-term needs with long-term goals
  • Provide overall management of day-to-day operations of assigned study (ies) to ensure completion per established program goals
  • Lead cross-functional teams and ensure vendors are compliant with contracted scope of work

Budget Management Vendor Management Communication Skills

13 jobs similar to Associate Director, Clinical Trial Management

Jobs ranked by similarity.

$155,000–$180,000/yr
US

  • Lead and manage the day-to-day operational execution of assigned cell therapy trials.
  • Develop and manage study timelines, budgets, forecasts, and related operational metrics.
  • Partner with external vendors / CROs / service providers to ensure high quality and timely deliverables.

Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for patients suffering from autoimmune diseases. They are committed to transforming the future of treatment for autoimmune disease and are guided by their core values.

US 3w PTO

  • Identify operational efficiencies for Apogee in partnership with key CROs and vendors and implement solutions to support delivery of Clinical Trial Operations team.
  • Partner with key stakeholders including Clinical Trial Operations, Vendor and Strategic Management to ensure vendor performance aligned with Apogee expectation.
  • Proactively identify and maintain standards to ensure consistency across all programs and studies for operationalizing global clinical trials working with assigned CRO’s.

Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets. They have a fast-paced company culture, founded on their C.O.R.E. values: Caring, Original, Resilient and Egoless and a commitment to refusing to stop at “good enough”.

US

  • Serve as leader of the local study team on assigned studies.
  • Manage and maintain accurate country level plans including timelines and budgets.
  • Implement startup and site activation plans at various levels.

Jobgether uses an AI-powered matching process to ensure applications are reviewed quickly, objectively, and fairly. They identify top-fitting candidates and shares this shortlist directly with the hiring company.

US

  • Provide strategic and administrative leadership for clinical research business and operational activities.
  • Ensure studies are conducted in accordance with regulatory requirements and sponsor expectations.
  • Drive operational performance, program growth, and team development across the clinical research enterprise.

Florida Cancer Specialists & Research Institute (FCS) has built a national reputation for excellence since 1984. With over 250 physicians, 220 nurse practitioners and physician assistants and nearly 100 locations, they utilize innovative clinical research, cutting-edge technologies, and advanced treatments.

$100,000–$120,000/yr
US

  • Lead clinical trial execution across the site network, overseeing study start-up, activation, and ongoing operational performance.
  • Serve as the primary operational liaison for Sponsors and CROs, providing regular updates on study progress, risks, and mitigation strategies.
  • Act as a central resource for site teams, resolving operational and protocol-related challenges and driving timely solutions.

Hawthorne Health is a leading community site network and home research visit solution provider, with 20+ sites and more than 2,000 research experienced healthcare professionals across the U.S. They leverage convenient, trusted, healthcare locations, identified patient data, and intelligent technology to accelerate patient access, improve retention, and reduce study costs.

$140,000–$170,000/yr
US

  • Responsibility for day-to-day activities within a region or regions, including site selection, start-up, maintenance, and close-out activities.
  • Serve as the key operational contact for Braveheart Bio studies aiding in site selection, study implementation, and ongoing coordination of study sites, either directly or via CROs.
  • Proactively identify potential operational challenges and, in collaboration with senior team members, provide solutions to ensure study execution remains on track.

Braveheart Bio is a Bay Area–based biopharmaceutical company pioneering best-in-class therapies for cardiovascular disease. With a proven leadership team, a strong financial foundation, and a high-value late-stage asset, Braveheart Bio represents an outstanding opportunity for ambitious, mission-driven professionals to make a tangible impact in a rapidly evolving therapeutic area.

$155,000–$183,000/yr

  • Responsible for operational oversight of the site, site health and monitoring activities.
  • Support sites in understanding study expectations, timelines, and required deliverables.
  • Build and maintain strong, trusted relationships with investigators and site staff.

CSL Behring is a global biotherapeutics leader committed to saving lives. They focus on serving patients’ needs by using the latest technologies to discover, develop, and deliver innovative therapies. CSL's parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people and delivers its lifesaving therapies to people in more than 100 countries.

US

  • Manages the financial, regulatory, patient management, and human resources functions associated with conducting clinical trials.
  • Supervises a staff of 2 - 5 employees; trains new clinical trials staff; tracks enrollment, sponsor payments, and salary.
  • Provides leadership in business development and assists residents in preparing research projects by facilitating IRB submissions and protocol writing.

Emory University is a leading research university fostering excellence and attracting world-class talent to innovate today and prepare leaders for the future. They welcome candidates who can contribute to the excellence of their academic community.

Europe

  • Management and operational delivery of clinical elements within a trial.
  • Successful execution of assigned trials and ensuring completion of deliverables.
  • Identify challenges to study timelines and offer creative action plans.

Precision for Medicine is a precision medicine CRO, integrating novel clinical trial designs, operational and medical experts, and biomarker and data analytics solutions. They are passionate about rare diseases and oncology, working across other therapeutic areas, with high-energy, dedicated professionals.

Europe

  • Lead, mentor, coach, and manage Clinical Trial Managers to support skill development and career growth.
  • Partner with Clinical Operations leadership and cross-functional teams to improve processes and quality.
  • Ensure compliance with SOPs, regulatory requirements, project plans, and quality standards.

Precision for Medicine is a clinical research company. They focus on improving the quality and productivity of clinical trial management operations.

US

  • Oversee and manage regional operational activities of global pivotal trials.
  • Develop and oversee procedures for troubleshooting and problem solving.
  • Maintain effective communication with vendors and internal departments.

Prilenia is a private biopharmaceutical company focused on developing transformative medicines for neurodegenerative diseases. With a highly committed and talented global team, they are developing pridopidine, an investigational neuroprotective therapy for ALS and Huntington’s disease.

US

  • Act as a program lead for the SVP, structuring ambiguous operational challenges, defining solutions, and driving high-impact initiatives from decision to execution.
  • Own the Clinical Ops leadership "front door," including intake and triage; run the operating rhythm and maintain core artifacts, including the OKR tracker and Initiative log.
  • Act as the critical link between Clinical Ops and partners (Quality/Safety, Product, Finance, HR) to unblock progress, resolve ownership/resourcing gaps, and coordinate complex rollouts.

Midi Health is a fast-scaling virtual care company focused on women’s health, transforming healthcare delivery through a modern, tech-forward platform and a distributed clinical team. The company seems to have a modern, tech-forward culture driven by innovation.

$100,675–$151,192/yr
Europe

  • Ensure the development and implementation of action plans.
  • Lead regional/therapeutic area project resourcing.
  • Develop, mentor, manage and coach GCM Managers.

Precision for Medicine is a global precision medicine clinical research services organization. They improve the clinical research and development process for new therapeutics by integrating clinical operations excellence, laboratory expertise, and advanced data sciences.