Oversee clinical operations for a project at a regional/global level, ensuring compliance with protocols and regulations.
Act as primary liaison between CRAs and clinical project team, providing training, oversight, and assessment.
Manage site performance, develop study tools, and support enrollment strategies to meet project timelines.
Alimentiv provides clinical services for global clinical trials, specializing in study delivery and monitoring. The company emphasizes quality, compliance, and professional growth, with a team of experienced professionals.
Provide therapeutic and operational leadership throughout the clinical program and project delivery lifecycle.
Collaborate with cross-functional teams to develop effective delivery strategies and resolve operational challenges.
Ensure clinical projects within the assigned franchise are appropriately resourced and aligned with operational goals.
Our partner is a global clinical research organization dedicated to advancing healthcare innovation and improving patient outcomes through high-quality clinical trials. They offer a collaborative and inclusive environment with experienced professionals across global therapeutic and operational teams, focusing on professional growth and meaningful impact.
Develop, mentor, coach and manage CTMs to progress their skillset per quality standards.
Collaborate with management to enhance CTM expectations and procedures for quality and efficiency.
Ensure CTMs have proper resources and training to deliver high-quality study conduct.
Precision for Medicine is a clinical research organization (CRO) that provides clinical trial management services. The company employs a large team of clinical research professionals and emphasizes quality and collaboration.
Support Clinical Trial Managers in the day-to-day execution of clinical trials from start-up through close-out.
Own critical study coordination workflows such as maintaining trackers, decision logs, and training records.
Ensure study documentation and training records are complete, current, and audit-ready.
Oura is a health technology company that produces the Oura Ring, a wearable device for tracking sleep, activity, and readiness. It is a quickly growing company with a mission-driven culture focused on employee well-being and innovation.
Serve as a subject matter expert for site management and monitoring strategies across complex clinical studies.
Collaborate with clinical teams, investigators, and stakeholders to ensure compliance, data quality, and trial success.
Mentor CRA staff, resolve escalated issues, and support site qualification, initiation, monitoring, and close-out visits.
Jobgether is a platform that uses AI-powered matching to connect candidates with job opportunities. They operate as a global healthcare and technology environment, offering professional growth and innovative solutions.
Act as a strategic partner for key customers, leading governance, growth initiatives, financial performance, and cross-functional collaboration.
Lead and oversee global, multiregional, or complex regional Clinical FSP partnerships, ensuring alignment with contractual agreements and strategic priorities.
Provide executive oversight for clinical FSP delivery, ensuring quality, timelines, key performance indicators, and contractual commitments are achieved.
The employer is a global clinical research organization that partners with pharmaceutical and biotech companies to deliver clinical trials. They are a large, established company with a culture focused on innovation, collaboration, and advancing healthcare worldwide.
Own and scale the patient engagement and recruitment strategy across a national site network, evolving the operating model to improve enrollment performance and patient experience.
Establish KPIs, dashboards, and reporting rhythms to drive recruitment performance across the patient funnel, using data to identify trends and resourcing needs.
Lead and develop the patient recruitment team, building a high-performing culture rooted in accountability, collaboration, and continuous improvement.
Profound Research partners with community physicians to offer clinical trials as a therapeutic option for their patients. As a growing organization, they foster a culture of compassion, urgency, solution orientation, and excellence, prioritizing patient-centered care and operational efficiency.
Monitor and own the progress of clinical studies at investigative sites, ensuring compliance with protocols, SOPs, ICH-GCP, and regulations.
Coordinate all necessary activities to set up and monitor a study, including investigator identification, regulatory submissions, and pre-study/initiation visits.
Identify potential study risks, propose solutions, and handle conflict using resolution strategies while maintaining quality and attention to detail.
Precision for Medicine, Oncology & Rare Disease is a precision medicine CRO that combines novel clinical trial designs, operational expertise, and biomarker analytics to advance oncology and rare disease treatments. The company fosters a culture with high CRA retention, small team influence, and a focus on work/life balance.
Support feasibility and study start-up activities for clinical research sites in Romania and Moldova, coordinating documents and site communication.
Maintain accurate trackers in Salesforce and Asana, flagging blockers and delays early to ensure timely site activation.
Serve as a day-to-day operational contact for sites, routing questions to appropriate internal, CRO, or sponsor contacts.
Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The company has 250+ employees worldwide and is headquartered in Cambridge, Massachusetts, and New York City, with a collaborative and low-ego team environment.
Acts as primary point of contact for trial-specific medical and safety questions, providing input to regulatory authorities and ethics committees.
Monitors participant safety, reviews protocol deviations and RAE reports, and supports pharmacovigilance with safety queries.
Participates in trial recruitment, investigator meetings, and reviews clinical study reports and essential trial documents.
PSI is a leading Contract Research Organization with over 30 years in the industry, focusing on delivering quality and on-time services across various therapeutic indications. They offer a balanced and stable yet innovative environment for employees, with an international team of medical professionals.