Lead data management activities for clinical trials, ensuring deliverables meet timelines and quality standards.
Create and review eCRF specifications, edit checks, and critical DM documents such as the Data Management Plan and Data Validation Plan.
Perform ongoing data review, reconciliation, database locks, and coordinate archiving of study databases.
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. With over 4,000 professionals in more than 20 countries, we maintain a quality-focused, collaborative one-team culture and below-average industry turnover.
Lead all aspects of clinical trial data management from study start-up to database lock for assigned projects.
Oversee database development, edit check specifications, data review, and quality control to ensure high-quality clinical data.
Serve as primary data management contact, coordinating with sponsors and vendors across LATAM and global teams.
Precision Medicine Group is a precision medicine and clinical research organization supporting the development of innovative therapies. They are building a growing LATAM Data Management team with a collaborative, quality-focused culture.
Lead data management activities for assigned clinical trials, ensuring quality and integrity of data.
Serve as subject matter expert on multidisciplinary teams and oversee CRO/vendor compliance.
Support temporary remote role requiring 20 hours/week and US work eligibility.
Penumbra is a global healthcare company focused on innovative therapies for challenging medical conditions. It designs, develops, manufactures, and markets novel products, and fosters a collaborative teamwork environment where learning is constant and performance is rewarded.
Lead and oversee clinical data management activities across assigned studies, ensuring high-quality data in compliance with ICH-GCP and company SOPs.
Manage CROs and external vendors, including database start-up, data cleaning, and database lock, while maintaining quality, timelines, and budget.
Collaborate cross-functionally with Biometrics, Clinical Operations, Medical, and other teams to drive data management milestones and inspection readiness.
We are developing novel biologics designed to set a new standard for the treatment of chronic skin diseases like plaque psoriasis. As a Nasdaq-listed startup, we foster a vibrant, inclusive culture where everyone is encouraged to bring their authentic selves to work.
Lead data management activities from study start-up to database lock, ensuring quality and timelines.
Act as subject matter expert for DM in sponsor meetings and implement process improvements.
Mentor and train junior DM staff while managing project documentation, data validation, and system setup.
Fortrea is a global contract research organization providing clinical development and biometrics services to pharmaceutical and biotechnology companies. With a focus on teamwork and excellence, they foster a family-like culture where employees collaborate to advance life-saving therapies.
Develop and manage case report forms (CRFs) for clinical studies.
Serve as liaison with database vendors and perform UAT.
Oversee data quality, support audits, and ensure regulatory readiness.
They develop innovative medical technology and manage clinical data for medical device studies. They operate in a fast-paced, collaborative environment with a focus on quality and regulatory compliance.
Serve as the primary clinical point of contact with clients, overseeing the operational portion of clinical studies per scope of work.
Develop study-related clinical documents, train CRAs and vendors, and lead internal clinical team meetings to ensure trial compliance.
Drive site feasibility, recruitment and retention strategies, and manage eTMF, budgets, and vendor oversight to ensure quality and timelines.
Precision for Medicine is a CRO that integrates clinical trial execution with deep scientific knowledge, laboratory expertise, and advanced data sciences to improve the speed, cost, and success rate of bringing life-changing therapies to patients, with a strong focus on Oncology and Rare Disease. The company combines new technologies, operational scale, and a collaborative environment to support the life sciences industry.
Manage all aspects of clinical trial data management from study start-up to post-database lock under supervision.
Oversee database development, testing, and quality control, ensuring compliance with SOPs and regulatory guidelines.
Coordinate with stakeholders, vendors, and sponsors to ensure timely and accurate data deliverables.
Precision for Medicine specializes in clinical data management and research services for drug and device development. The company values accuracy, teamwork, and adherence to regulatory standards.
Lead a centralized team of Data Coordinators to ensure accurate, timely, and complete clinical research data.
Manage workload, quality, and compliance for data activities across the Care Access site network.
Partner with clinical operations, sponsors, and CROs to resolve data issues and improve processes.
Care Access brings clinical research and health services directly to communities through hundreds of research locations and mobile clinics. They are dedicated to making health care more accessible and put people at the heart of medical progress.
Manage post-visit data uploads, reviews, and quality checks for clinical research projects within specified timelines.
Communicate with in-house cardiology and sonography teams on data timelines and corrections, resolving data queries and performing quality checks.
Train, mentor, and coach sonographers while maintaining project documentation and supporting database lock activities.
Hawthorne Health is a community-based clinical research network and home research visit solution provider with 20+ sites and over 2,000 research-experienced healthcare professionals across the U.S. By embedding high-quality research within local communities, they make clinical trials more accessible and convenient for patients.
Lead ongoing clinical data review to ensure quality, interpretation, and patient safety across development programs.
Develop and review study protocols, investigator brochures, and regulatory documents in partnership with cross-functional teams.
Represent Clinical Development on study teams and present clinical data and scientific information to internal and external audiences.
Deciphera, a member of Ono Pharmaceutical Co., Ltd., is a biopharmaceutical company discovering, developing, and commercializing new medicines for cancer, neurologic, and autoimmune disease. They cultivate an inclusive culture valuing curiosity, creativity, and shared accountability, empowering individuals to challenge the unknown together.
Review source data from clinic visits and perform quality control to ensure completeness and consistency before entry into sponsor EDC/CRF systems.
Reconcile study data against supporting documentation and track missing or inconsistent records through to resolution.
Enter study data into EDC/CRF systems accurately and manage queries, following up with site teams to resolve issues.
Care Access brings clinical research and health services directly to communities, using hundreds of research locations and mobile clinics to make trials more accessible. The company emphasizes an inclusive culture where diverse backgrounds are valued and people are at the heart of medical progress.
Lead feasibility assessments for client proposals and clinical trial planning.
Review protocols and operational plans to develop evidence-based recommendations.
Present findings and rationales to internal teams and clients to support decision-making.
Precision for Medicine combines clinical-trial execution, scientific expertise, and data sciences to accelerate clinical development. The organization focuses on oncology and rare diseases and operates across Europe, the US, and globally.
Oversee evidence-generation strategy and manage research studies for the da Vinci Cardiac Surgery Program.
Collaborate with stakeholders to identify evidence gaps, align priorities, and develop evidence-generation plans.
Manage CROs, research partners, and publications while ensuring regulatory compliance and audit readiness.
Intuitive is a global leader in robotic-assisted surgery and minimally invasive care, with technologies like the da Vinci system transforming care for millions worldwide. We are a team of engineers, clinicians, and innovators united to make surgery smarter, safer, and more human.
Conduct outbound and inbound calls to prospective clinical trial participants and perform protocol-specific prescreening.
Manage patient recruitment pipelines across multiple trials, including cardiology, vaccine, migraine, obesity, and diabetes studies.
Maintain accurate documentation of patient interactions and follow up with qualified candidates to support enrollment goals.
UniTriTeam is a clinical research organization focused on patient recruitment and prescreening for clinical trials. The team supports multiple concurrent studies across therapeutic areas including flu vaccines, migraine, obesity with diabetes, and cardiology, with a collaborative and patient-centered culture.
Partner with cross-functional teams and study sites to support clinical operations across all trial phases.
Perform remote monitoring of clinical trials and serve as secondary contact for sites supporting CRAs.
Ensure proper reporting and follow-up of SAEs, address non-compliance issues, and assist with audit/inspection readiness.
Premier Research is a global clinical research, product development, and consulting company helping biotech, specialty pharma, and MedTech innovators turn breakthroughs into new treatments. The company fosters a collaborative culture focused on agility, continuous learning, and making an impact.
Leads the planning, execution, and delivery of complex global clinical studies, managing timelines, budgets, and quality.
Oversees CROs and external vendors, ensuring alignment with study timelines, budgets, and contractual obligations.
Drives cross-functional collaboration and communicates study progress, risks, and decisions to stakeholders.
Deciphera, a member of Ono Pharmaceutical Co., Ltd., is a biopharmaceutical company focused on discovering, developing, and commercializing new medicines for cancer, neurologic, and autoimmune diseases. The company cultivates an inclusive culture that values curiosity, creativity, and shared accountability, empowering individuals to challenge the unknown together.