Act as primary clinical point of contact with clients and lead planning, execution, and oversight of clinical studies across Latin America.
Develop country-level recruitment strategies, guide monitoring and quality strategies, and mentor CRAs and partners.
Collaborate with project managers on budgets, vendor management, and ensure compliance with ICH-GCP and regulatory requirements.
Precision Medicine Group is a precision medicine company that provides clinical research and commercialization services. The company is an Equal Opportunity Employer with a focus on expanding clinical operations across Latin America.
Conduct inbound and outbound calls to prospective clinical trial participants and perform prescreening interviews.
Educate participants about clinical research and schedule eligible candidates for screening appointments.
Maintain accurate documentation and meet productivity and quality metrics in a remote environment.
Jobgether is a platform that uses AI-powered matching to connect candidates with job opportunities. They operate with a collaborative international team and focus on efficient, fair hiring processes.
Acts as primary site contact and liaison for study management issues, ensuring compliance with ICH-GCP and regulatory requirements.
Manages essential document collection, maintenance, and TMF organization, and coordinates investigator recruitment activities.
Assists with data review, EDC entry, and supports offsite central monitoring and study supply management.
Precision Medicine Group is a clinical research organization providing services to pharmaceutical and biotech companies. The company has a global presence and fosters a collaborative culture focused on precision medicine.
Manage global clinical trial operations, ensuring adherence to timelines, budget, and quality standards.
Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures.
Build and manage strong relationships with trial investigators and stakeholders, ensuring regulatory compliance.
ICON is a global healthcare intelligence and clinical research organization that helps bring new medicines and treatments to patients faster. It is a values-driven company with a focus on integrity, collaboration, agility, and inclusion, employing a diverse global workforce.
Responsible for phone screening, scheduling, and tracking recruitment for clinical trials.
Make 60+ outbound calls daily, assess participant eligibility, and enter data into databases.
Requires bilingual English/Spanish preferred, customer service experience, and strong communication skills.
Headlands Research is a leading network of advanced clinical trial sites, leveraging cutting-edge technology and support services to enhance community outreach and participation. Founded in 2018, the company operates 20+ sites across the US and Canada and is rapidly expanding.
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.
Serve as primary point of contact for customers during the pre-trial phase of AAC device trials.
Conduct engagement conversations via calls, email, and chat to educate caregivers and clinicians on Lingraphica's offerings.
Ensure accurate documentation of customer interactions in CRM and contribute to monthly intake goals.
Lingraphica is a mission-driven organization that provides speech-generating devices to improve communication for people with impairments. They are a leader in AAC technology, serving aphasia patients, and foster a fast-paced, goal-oriented culture.
Lead the development of investigator grant budgets and oversee the grant administration team globally.
Manage clinical site budgeting tools and ensure timely and accurate investigator payments.
Contribute to month-end close processes and provide guidance on clinical trial agreements.
Precision Medicine Group is a global life sciences company specializing in clinical research and precision medicine. The company is expanding its team in LATAM and fosters a collaborative, high-energy culture focused on excellence and continuous improvement.
Lead the development and optimization of clinical data systems, driving data standardization and building scalable validation frameworks.
Architect high-performance databases and ETL pipelines, integrating data from diverse clinical systems across global trials.
Serve as a strategic liaison between Biostatistics, Clinical Operations, and Regulatory Affairs to translate clinical requirements into technical solutions.
Precision Medicine Group is a specialized life sciences company that accelerates the development and delivery of precision medicine. It has a global workforce and fosters a collaborative, compliance-oriented culture focused on innovation and regulatory excellence.
Manage the identification, outreach, and onboarding of high-performing clinical sites into the North America ASN.
Develop strong relationships with high-priority sites and partners to expand the site network.
Build innovative solutions to grow a pipeline of high-potential sites and enhance clinical trial delivery.
Alimentiv is a clinical research organization that drives clinical trial delivery through site network management. They are a global company with a focus on operational excellence and innovation.
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.
Provides study-level oversight and leadership for global clinical trials from inception through closure, managing vendors, recruitment, and cross-functional teams.
Develops and manages study materials including protocols, regulatory submissions, and budgets while ensuring compliance with quality standards and inspection readiness.
Contributes to system management like EDC, IRT, and eTMF, and supports process improvement initiatives or serves as a mentor.
AbbVie discovers and delivers innovative medicines and solutions to address serious health issues in immunology, oncology, neuroscience, and aesthetics. As a global biopharmaceutical company with a robust pipeline, they emphasize integrity and innovation, serving patients worldwide with a dedicated team.