Source Job

• 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.

• 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.

• Lead strategic account management initiatives and develop access strategies for public and private healthcare systems in Brazil.
• Build strong relationships with payers, hospitals, and government stakeholders to expand patient access to treatments.
• Coordinate multidisciplinary teams and manage account performance to drive sustainable business growth.

Jobgether uses an AI-powered matching process to connect candidates with hiring companies. They are a global platform focused on efficient and objective recruitment, with a culture of inclusion and innovation.

• 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.

• Perform in-house and remote monitoring activities for clinical trials, ensuring compliance with regulatory requirements and study protocols.
• Support study start-up, site selection, and document tracking while assisting CRAs with on-site and remote monitoring.
• Communicate with investigative sites to resolve queries and maintain study tracking tools for deviations, SAEs, and data discrepancies.

Jobgether is an AI-powered job matching platform that connects candidates with hiring companies. The environment is collaborative, international, and focused on improving patient outcomes through high-quality research.

• 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.

• Manage a team of 15-17 Study Management Associates (SMAs) to deliver best-in-class study execution.
• Drive performance management, mentoring, and professional development for direct reports.
• Support resource management, adherence to regulations, and continuous process improvements.

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. The company operates across several therapeutic areas including immunology, oncology, and neuroscience, with a significant global presence and a culture focused on innovation and impact.

• 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.

• Provide study oversight as primary liaison between CRAs, internal staff, site staff, client personnel, and external vendors.
• Ensure clinical monitoring activities comply with SOPs, regulations, GCP, KPIs, and study-specific requirements.
• Develop and manage clinical plans and guidelines, including the clinical monitoring plan and study timelines.

ProTrials is a women-owned, WBENC-certified Contract Research Organization (CRO) that has been a trusted partner in clinical research since 1996, supporting research behind innovative treatments in pharmaceutical, biotech, and medical device industries. They foster a collaborative community where team members feel valued, supported, and empowered to make a meaningful impact on global health.

• Provide strategic oversight and leadership for a portfolio of complex global clinical trials in dermatology and rheumatology.
• Serve as the key client contact, ensuring alignment on objectives, communication, and satisfaction throughout the study lifecycle.
• Monitor budgets, timelines, risks, and quality while mentoring project managers and driving operational improvements.

The company is a specialized Contract Research Organization (CRO) focused on dermatology and rheumatology clinical trials. It fosters an international, collaborative, and science-driven environment with a commitment to operational excellence and innovation.

• Drive the product lifecycle for clinical trials digital tools, from concept to launch, ensuring fit-for-purpose solutions that meet end user needs.
• Coordinate market research and customer insights to define product features, prioritize the roadmap, and balance customer value with business impact.
• Collaborate with engineering, product owners, and stakeholders across geographies to deliver SaaS products in a regulated environment.

Cogstate advances the science of brain health by making cognitive assessment faster, easier, and more accurate for clinical trials, healthcare, and everyday life. Their global team of experts works across psychology, data science, operations, and technology with a patient-first mindset, supporting over 2,000 clinical trials in more than 150 countries.

• Lead clinical trial support services and site engagement strategy to maximize patient participation.
• Orchestrate cross-functional teams to translate partner needs into scalable, data-driven programs.
• Act as principal medical point of contact for pharma partners, driving contract negotiation and patient impact.

Natera is a global leader in cell-free DNA testing, dedicated to oncology, women's health, and organ health. The Natera team consists of highly dedicated professionals from world-class institutions, who care deeply for our work and each other.

• 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.

• Lead and mentor a high-performing team of Clinical Research Associates, ensuring operational excellence and efficient resource utilization.
• Manage hiring, onboarding, performance management, and professional development activities for CRA staff.
• Collaborate with Project Managers and cross-functional teams to support successful delivery of clinical trials.

PSI is a leading Contract Research Organization with more than 30 years in the industry, offering a balance between stability and innovation. They focus on delivering quality and on-time services across various therapeutic indications.

• 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.

• Serves as clinical trial lead, overseeing study planning, conduct, and oversight per protocol and regulations.
• Develops study documents, manages site feasibility, and drives recruitment strategies.
• Leads internal clinical team meetings and ensures quality deliverables through metric reporting.

Precision Medicine Group is a life sciences company that supports clinical research and development. The company is large enough to offer a range of benefits and emphasizes a collaborative, ethical culture focused on quality and compliance.

• Manage and oversee all clinical aspects of trials across multiple countries, ensuring timeline adherence, quality, and scope.
• Lead CRAs and collaborate with cross-functional teams to achieve high client satisfaction and smooth trial operations.
• Identify risks, develop creative action plans, and maintain focus on study priorities through effective communication.

Precision for Medicine is a precision medicine CRO that combines novel trial designs, advanced biomarker analytics, and deep oncology expertise to accelerate drug development. The company fosters a dynamic, high-energy culture and values dedicated professionals who thrive in challenging environments.

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborating with investigators and site staff to facilitate smooth study conduct.

ICON is a global healthcare intelligence and clinical research organization dedicated to accelerating the development of new medicines and treatments. As a values-driven company, ICON fosters a culture of integrity, collaboration, agility, and inclusion, employing a diverse workforce.

• 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.

• Serve as both a practicing clinician and clinical leader, managing Clinical Leads and driving clinical quality and performance.
• Chair the Credentialing Committee, act as a collaborating/supervising physician for nurse practitioners, and participate in direct patient care with a 1-in-2 on-call schedule.
• Collaborate across Operations, Product, Engineering, Legal, and Compliance to support safe and effective AI integration into clinical care.

Curai Health is an AI-enabled, fully virtual medical group making high-quality, asynchronous primary care accessible at scale. They are a mission-driven team of talented colleagues committed to living their values and driving meaningful impact in healthcare.