Source Job

• 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.

• 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.

• Define and document data integration requirements between systems, ensuring clear specifications for data exchange.
• Analyze data sources and establish authoritative sources, resolving conflicts and supporting data quality.
• Collaborate with product managers and clinical stakeholders to translate feasibility needs into platform requirements.

Bertoni Solutions is a multinational technology consulting firm that helps businesses leverage technology for success. Founded in 2016, the company combines Swiss organizational skills with Latin American talent and passion.

• Act as the technical authority on clinical data structures, standardizing and harmonizing data pipelines with global partners.
• Write production-grade Python code to automate data cleaning, enforce quality control, and design data dictionaries for AI models.
• Map clinical data to industry-standard ontologies (e.g., SNOMED, ICD) with a focus on oncology and immunology datasets.

Bioptimus is building the first universal AI foundation model for biology to accelerate innovation in biomedicine. With over $75M in funding, it is a fast-growing startup headquartered in Paris with a world-class team of scientists and engineers.

• 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.

• Lead sponsor-side clinical data management activities across CoMind's clinical development portfolio.
• Design, build, and configure clinical study databases including eCRF design and database validation.
• Serve as subject matter expert on regulatory expectations and manage vendor relationships.

CoMind develops non-invasive neuromonitoring technology for clinical brain monitoring. The company is an early-stage startup with an AI-driven culture.

• Develop long-term technical vision and design scalable data systems.
• Build and maintain production data pipelines using Python and integrate external APIs.
• Mentor engineers and uphold standards for engineering excellence.

Correlation One is the largest provider of AI and data workforce development programs globally, having trained over 500,000 professionals across 11 countries. They work with Fortune 500 enterprises and government agencies to close skills gaps, and foster a culture of empowerment and diversity.

• Works as a positive team member to deliver quality data applications within scope, on time, and within budget.
• Develops strategies for managing complex data sets and integrates disparate data sources for improved reporting.
• Mentors other analysts on regulation adherence and follows HIPAA standards.

Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate today and prepare leaders for the future. The organization offers a diverse and inclusive environment, with a focus on academic excellence and equal opportunity.

• Ensure timely review, processing, and quality of Trial Master Files (TMF) according to GCP and SOPs.
• Create and execute study TMF plans, manage document indexing, and communicate changes to project teams.
• Monitor TMF health, identify risks, and support audits and inspections for compliance.

Precision Medicine Group is a global contract research organization providing clinical trial support and precision medicine services. The company values professionalism, collaboration, and quality, with a focus on maintaining inspection-ready trial master files.

• Lead design and ownership of scalable data pipelines using SQL, Python, dbt, and cloud-native tools on Snowflake.
• Architect and optimize Snowflake environments, including cost governance, performance tuning, and cloud integration.
• Enforce data governance frameworks, security protocols, and data quality standards across the platform.

BlueCloud is a Snowflake Elite Partner and 2026 CoCo Catalyst Partner of the Year, helping enterprises migrate to AI-ready Snowflake platforms. With 450+ consultants and 200+ transformations, they deliver data solutions 40–50% faster across multiple industries.

• Maintains responsibility for all assigned biostatistics duties within clinical studies, including acting as study lead for multiple or complex studies.
• Reviews and develops clinical program designs, protocols, and statistical analysis plans, ensuring high-quality and valid content.
• Provides mentoring to junior statisticians and represents the biostatistics function in internal and external meetings and audits.

Ergomed Group is a rapidly expanding full-service mid-sized CRO specialising in Oncology and Rare Disease. Since 1997, the company has grown organically with operations in Europe, North America and Asia, fostering a true international culture that values employee experience, well-being, and work-life balance.

• 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.

• Own data pipeline development. Build and maintain reliable pipelines that ingest, transform, and deliver healthcare data across the organization.
• Design warehouse data models. Create scalable schemas and data structures that support analytics, reporting, and evidence generation.
• Lead data transformation strategy. Establish frameworks and standards that improve consistency, maintainability, and performance.

Pivotal Health builds a technology platform to help healthcare providers get paid fairly in complex reimbursement landscapes. The company is a collaborative, low-ego team on a mission to make healthcare reimbursement fairer.