Interpret clinical diagnostic testing results in accordance with established SOPs.
Independently draft clear, accurate clinical testing results.
Maintain expertise in clinical and technical aspects relevant to the specific position.
Ambry Genetics Corporation is a CAP-accredited and CLIA-licensed molecular genetics laboratory based in Aliso Viejo, California. They are a genetics-based healthcare company dedicated to open scientific exchange to understand and treat all human disease faster. At Ambry, employees are learning, challenging themselves, and having fun while collaborating with teammates through the open exchange of ideas.
Develop client-ready deliverables including protocols, statistical analysis plans, and technical reports.
Manage the delivery of project components by collaborating with other staff members.
Contribute to development of proposals and presentations under guidance of senior team members.
Precision Medicine Group is a portfolio organization that helps its clients with sophisticated evidence synthesis projects. The company has a start-up culture with vision in its field.
Collaborate with CROs to develop and optimize IHC assays.
Translate biological questions into quantitative image-based endpoints.
Provide mechanistic insights in CAR-T infiltration and immune activation.
Legend Biotech is dedicated to treating life-threatening diseases. They are developing advanced cell therapies across a diverse array of technology platforms and have three R&D sites around the world.
Perform statistical analyses on behavioral, electrophysiological, and imaging datasets.
Process and clean raw data, maintaining organized, well-documented data files and analysis pipelines.
Develop figures, graphs, and visualizations of project results for manuscripts, presentations, and grants.
The Opendak Lab conducts neuroscience research. While the job posting does not specify lab size or culture we infer that the lab is currently undergoing a research project.
Supports all phases of clinical development and execution.
Ensures high quality data by being the study protocol expert and key site resource for questions.
Maintains and tracks clinical study data and supports investigator qualification selection.
SI-BONE is a medical device company focused on minimally invasive sacropelvic solutions. They aim to help patients with sacroiliac pelvic conditions and have provided over 90,000 procedures to date using their iFuse Implant System.
Contribute to the design and planning of clinical and real-world evidence studies.
Create and maintain scientific and operational documentation and tools to support Oura’s clinical and real-world evidence studies.
Support data-driven insights generation through organizing, summarizing, and describing health-related data.
Oura's mission is to empower every person to own their inner potential. Their award-winning products help their global community gain a deeper knowledge of their readiness, activity, and sleep quality by using their Oura Ring and its connected app. As a quickly growing company focused on helping people live healthier and happier lives, they ensure that their team members have what they need to do their best work — both in and out of the office.
Provide statistical support for Phase I–IV clinical trials.
Participate in protocol development, study design, and sample size calculations.
Prepare and review Statistical Analysis Plans (SAPs), TLF shells, and randomization specifications.
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. They have over 4,000 professionals in more than 20 countries with a mission to contribute to a healthier and safer world.
Represent the Biostatistics function for complex studies or at project level.
Independently contribute to design of early/late-stage protocols across multiple therapeutic areas and help draft protocols or amendments.
Develop and write statistical analysis plans and perform statistical analyses for interim and final reports to be submitted to regulatory agencies.
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. They have over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.
Contribute to the design of early/late-stage protocols across multiple therapeutic areas.
Develop and write statistical analysis plans, and perform statistical analyses for interim and final reports.
Support submission activities, including design, analysis and reporting of integrated summaries for safety and efficacy.
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, they focus on quality, professional development, and a supportive culture.
Define and execute the scientific vision and R&D roadmap aligned with company milestones.
Oversee lead preclinical programs in focus indications, such as tRNA elevation in neuromuscular diseases.
Drive IND-enabling studies, including biodistribution, toxicology, and dose-finding.
XtRNA Bio is a pioneering biotechnology company developing a proprietary tRNA therapeutic platform for underserved patients with rare genetic diseases and high unmet medical needs. They are advancing a novel approach to correct translational defects at their root, from discovery through to the clinic — with a focus on meaningful, durable benefit for patients who currently have no options.