Serve as the primary point of contact for assigned protocols, linking Country Operations with the clinical trial team.
Manage project timelines, deliverables, and performance for clinical studies from feasibility to close out.
Ensure compliance with ICH/GCP, country regulations, and company policies while leading local study teams.
Merck is a global healthcare leader with a diverse range of prescription medicines, vaccines, and animal health products. With over 100 years of history, the company employs tens of thousands worldwide and fosters a culture of innovation and inclusivity.
Manage site activation and regulatory submissions for clinical trials in Spain.
Oversee contract and budget negotiations with sites to ensure timely approvals.
Collaborate with cross-functional teams to maintain project documentation and timelines.
Precision for Medicine is a global Clinical Research Organization specializing in precision medicine for rare diseases and oncology. The company is experiencing continued growth and values operational excellence and regulatory expertise.
Serve as the primary clinical point of contact for clients and lead the operational conduct of clinical studies.
Develop study-related clinical documents, train CRAs, and drive site feasibility and recruitment strategies.
Oversee study submissions, monitoring, data quality, and vendor management, ensuring compliance with GCP and regulatory requirements.
Precision for Medicine is a CRO that integrates clinical trial execution with scientific expertise and advanced data sciences, focusing on Oncology and Rare Disease. They leverage new technologies and operational scale to improve the speed and cost of bringing therapies to patients.
Conduct and report all types of onsite monitoring visits, perform CRF review, source document verification, and query resolution.
Be responsible for site communication and management, supervise study activities, timelines, and schedules on the country level.
Support regulatory team in preparing documents for study submissions and participate in feasibility research.
PSI is a leading Contract Research Organization with over 30 years of experience, offering a balance of stability and innovation. The company focuses on delivering quality and on-time services across a variety of therapeutic indications.
Synthesize participant behavioral data into clear, actionable insights for clinical stakeholders.
Map and analyze end-to-end digital trial experiences to identify friction and drop-off points.
Partner with clinical operations and UX to drive test-and-learn strategies for recruitment optimization.
New Era Technology provides end-to-end technology solutions, securely connecting people, places, and information at scale. With a global team of over 3,000 professionals, they foster a team-oriented culture that prioritizes personal and professional development.
Lead portfolio-level financial analysis for Clinical Solutions departments, including forecasting, budget health, and margin performance.
Perform variance analysis and monitor trial operations KPIs to link operational performance to financial outcomes.
Leverage Excel and Power BI to create dashboards and executive-ready materials for senior leadership.
Precision Medicine Group is a healthcare services company specializing in precision medicine and clinical research solutions. It operates in a collaborative, matrixed environment focused on delivery excellence and equal opportunity.
Support the design and execution of systematic literature reviews and evidence synthesis projects.
Conduct structured searches across bibliographic databases and supervise junior colleagues on screening and data extraction.
Manage multiple concurrent projects and contribute to client-facing deliverables including reports, manuscripts, and presentations.
This organization provides epidemiology, health economics, and outcomes research consulting to life sciences companies. It offers a collaborative, global, and intellectually engaging environment where quality, scientific rigor, and innovation are valued.
Evaluate RFPs and contribute to bid strategies for clinical supply proposals.
Collaborate with business development, contracts, proposals, and operations teams to align budgets and assumptions.
Manage multiple priorities in a fast-paced international environment while maintaining quality and accuracy.
This partner company operates in the clinical research and supply chain environment, supporting high-quality proposals and clinical trial supply management. It provides a fully remote, supportive working environment with a focus on employee health and wellbeing, offering exposure to international projects and collaboration with cross-functional teams.
Collect, review, and prepare site and regulatory documentation for UK clinical trial submissions.
Support regulatory submission preparation and ICF adaptations in compliance with ICH-GCP and local regulations.
Liaise with investigative sites to obtain, track, and resolve outstanding documentation and maintain study tracking systems.
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We seek out diverse talent with a relentless commitment to innovation and impact.
Lead and support statistical programming deliverables for oncology clinical studies.
Ensure high-quality programming with CDISC standards and regulatory compliance.
Collaborate with cross-functional teams including statisticians, data managers, and study leaders.
ClinChoice is a global full-service CRO specializing in clinical development for pharmaceutical, biotechnology, medical device, and consumer health companies. They have over 28 years of experience and over 4,000 professionals in more than 20 countries, with a culture focused on quality, professional development, and supportive collaboration.
Develop Clinical Evaluation Plans (CEPs) and Clinical Evaluation Reports (CERs) per EU MDR to support CE Mark submissions.
Interact with cross-functional teams to define strategies for clinical documentation and regulatory submissions.
Conduct literature searches, critically appraise scientific data, and write clinical summaries for products and surgical procedures.
Intuitive is a global leader in robotic-assisted surgery and minimally invasive care, developing technologies like the da Vinci surgical system and Ion to transform surgery. The company is a team of engineers, clinicians, and innovators united by a purpose to make surgery smarter, safer, and more human, with challenging but deeply meaningful work.
Conduct quantitative analyses on Novellia's patient datasets with support from the solutions team.
Translate analytical findings into scientific communications materials including white papers, abstracts, and media summaries.
Maintain rigorous standards for data integrity and ethical use of patient data.
Novellia is a patient-powered real-world data platform that provides comprehensive health insights to accelerate biopharma innovation. The company is growing 5x year-over-year, backed by top investors, and is dedicated to building a diverse, inclusive, and authentic workplace.
Review, draft, and negotiate a variety of legal agreements including clinical study agreements and confidentiality agreements.
Work closely with Clinical Operations study teams to ensure contract deliverables align with study timelines.
Establish, track, and report site contract metrics and support contract file maintenance.
Precision for Medicine provides clinical research services to the pharmaceutical and biotechnology industries. The company is part of Precision Medicine Group and fosters a collaborative culture focused on precision medicine.
Serve as a bridge between business stakeholders, clinical teams, and technology partners to identify process improvements and implement AI-enabled solutions.
Gather and document requirements, coordinate testing and user feedback, and drive adoption of new technologies like Microsoft Copilot.
Support development of AI agents, prompt libraries, SOPs, and other resources to help teams leverage emerging technologies effectively.
Precision Medicine Group is a company that provides specialized services to the life sciences industry, focusing on precision medicine. They are a large organization with a culture that values innovation and collaboration, operating in a matrixed environment.
Assist the BD team in preparing proposal responses for high-priority opportunities, working with clinical subject matter experts to create customized responses and budgets.
Support costing by generating initial assumptions, populating CRO costings, and ensuring rolled-up costing accuracy.
Contribute to general BD support including bid/no bid meetings, client presentations, and continuous improvement of BD tools.
Alimentiv is a global clinical research organization that provides clinical trial services to the pharmaceutical and biotechnology industries. The company fosters a collaborative culture and supports continuous improvement.
Assist in preparing clean databases by reviewing clinical trial data through CDMS or external data listings to ensure compliance with protocols.
Generate queries to resolve data discrepancies and support the development of CRFs and edit check specifications.
Maintain documentation related to CRF and data listing testing, including user acceptance testing.
Premier Research is a global clinical research, product development, and consulting company that helps biotech and specialty pharma transform life-changing ideas into new medical treatments. The company values teamwork, agility, and care for patients, providing a diverse culture with opportunities for growth and continuous learning.
Own the end-to-end proposal development process across a multi-million-dollar book of business.
Translate client needs into clear, tailored proposals aligned with budgets and timelines.
Support smooth delivery during fieldwork by handling clarifications and objections.
Konovo is a global healthcare intelligence company transforming research through technology, providing access to over 2 million healthcare professionals and patients. With over 200 employees across five countries, it fosters a collaborative, remote, and fast-paced culture transitioning from service to product-driven platform.
Produce business and market intelligence by querying data repositories and generating periodic reports to identify patterns and trends.
Clean, transform, and analyze data to create key business insights and support recommendations for action.
Manage raw data, create databases, and analyze data using statistical methods to present clear summaries.
WCG delivers transformational solutions that accelerate clinical research and advance human health. They serve experts on the frontlines of science and medicine, investing in their people with comprehensive benefits and career development opportunities.
Responsible for site activation readiness, submission preparation, and interaction with Competent Authorities and Ethics Committees.
Manage essential document collection, informed consent customization, and maintain project plans and trackers.
Partner with cross-functional teams and act as subject matter expert for country-specific regulatory knowledge.
We are a global life sciences company specializing in clinical trial regulatory and start-up services. We are expanding our capabilities across Latin America and seek experienced professionals to join our team.
Prepare and maintain Trial Master Files for internal and external studies to meet sponsor specifications.
Communicate with sponsors, project managers, and study contacts to ensure compliance with protocols and regulatory requirements.
Manage multiple priorities and ensure file structure and indexing are accurate.
Celerion is a clinical research organization that uses translational medicine to accelerate drug development. The company values integrity, trust, teamwork, and respect, and is an equal opportunity employer.