Source Job

• Provide clinical case coverage and train surgical teams on safe and effective device use.
• Manage inventory, reconcile usage, and ensure compliance with company policies.
• Collaborate with sales teams and support physician training and education programs.

Calyxo, Inc. is a medical device company focused on improving kidney stone treatment. Founded in 2016 and headquartered in Pleasanton, California, the company is led by experienced executives and investors with a proven track record of commercializing innovative urology devices.

• Deliver clinical education and training to physicians and hospital staff during surgical study cases in the US.
• Plan activities to support recruitment at sites and ensure compliance with clinical protocols and regulations.
• Support multiple studies with different protocols and travel up to 70% within the Central US region.

Kuros Biosciences is a Swiss-headquartered biotech company focused on advancing bone healing with high-quality scientific evidence. With operations in the Netherlands and the USA, we continue to grow our global team and have a commercial and research footprint spanning over 20 markets.

• Conduct validation studies on Chemistry and Immunoassay diagnostic instruments for customer laboratories.
• Provide onsite and remote technical support, training, and troubleshooting for assay and quality-control issues.
• Collaborate with internal teams and travel extensively to support customers across the Northeastern US.

They provide Chemistry and Immunoassay diagnostic instrumentation and support services to healthcare laboratories. Their culture emphasizes customer education, technical validation, and collaborative teamwork across field service, sales, and training teams.

• Provide procedural support to new users to promote safety and effective progression through learning curves.
• Support training activities including in-services, training labs, and development of teams and programs.
• Collaborate with sales teams and hospital staff to integrate Ion® at new customer sites.

Intuitive is a global leader in robotic-assisted surgery and minimally invasive care, transforming how care is delivered for millions of patients worldwide. The company is a team of engineers, clinicians, and innovators united by a purpose to make surgery smarter, safer, and more human.

• Manage day-to-day operations for the outpatient clinical documentation improvement program across multiple facilities.
• Liaise with physicians and leadership on coding rules, risk adjustment, and reimbursement guidelines.
• Ensure compliant and accurate medical record documentation while facilitating standardization.

Henry Ford Health is an academic health system providing comprehensive care across Michigan. With 12 hospitals and hundreds of clinics, it is a large organization focused on collaboration and innovation.

• Lead cross-site technology transfer, cleaning validation, and process validation for sterile and nonsterile manufacturing operations.
• Serve as the go-to technical resource for diagnosing and resolving process deviations, yield losses, and quality issues across four sites.
• Manage and develop site Technical Services Managers, setting network-wide standards and ensuring consistency in validation and troubleshooting.

Hims & Hers is a leading health and wellness platform that redefines healthcare by providing affordable, accessible, and personal care from diagnosis to treatment to delivery. As a publicly traded company on the NYSE, it fosters a culture of innovation, normalizing health challenges, and supports a talent-first flexible/remote work approach.

• Provide remote and on-site support and repair for customers across the Americas, acting as the subject matter expert for the product line.
• Coach and mentor partner technicians, lead technical projects, and conduct training classes for technicians.
• Manage pre-installation assessments, preventative maintenance, parts returns, and maintain close communication with service managers.

FUJIFILM North America Corporation is the largest graphic distributor in the US, delivering digital printing and office solutions. The company has over 70,000 employees globally and offers a collegial culture and flexible work environment.

• Manage the intake, review, analysis, and reporting of Individual Case Safety Reports (ICSRs) and support Clinical Events Committees and Data Monitoring Committees.
• Co-author and maintain study-specific safety documents and prepare aggregate safety reports for regulatory submission.
• Collaborate with sponsors, study teams, and cross-functional partners to ensure data quality and compliance with GCP and GVP standards.

This partner company delivers high-quality safety services across clinical research and medical device programs. They foster a collaborative, detail-oriented environment with a focus on compliance and patient outcomes.

• Provide in-field technical applications support for automated histology instrumentation, reagents, and related solutions across the South Florida territory.
• Conduct installations, evaluations, qualifications, and optimization activities while delivering post-purchase training to promote effective product adoption.
• Build trusted technical relationships with customers and collaborate with commercial, technical service, and product teams to resolve challenges and support regional sales goals.

Our partner is a life sciences company focused on advancing diagnostic technologies and improving patient care through innovative histology instrumentation and reagents. They offer a collaborative environment with opportunities for professional growth and customer-facing experience.

• Orchestrate the flow of coded medical record information across inpatient and outpatient settings for billing accuracy.
• Champion data quality by monitoring completeness, accuracy, and timeliness of medical documentation and coded submissions.
• Design and deliver educational programs for clinical providers and coding staff on best practices, compliance, and documentation improvement.

Henry Ford Health is a leading academic health system providing a comprehensive continuum of care across Michigan and beyond. With 12 hospitals and hundreds of ambulatory locations, they foster a culture of purpose, collaboration, and belonging, empowering team members to grow their careers and make a meaningful difference.

• Review CMC sections of regulatory submissions for drug-device combination products, ensuring accuracy and alignment with global requirements.
• Contribute to global regulatory CMC strategies and provide guidance to cross-functional stakeholders.
• Collaborate with device development, quality, clinical, human factors, and other teams to support product compliance and change controls.

The company specializes in drug-device combination products and operates in a cross-functional, science-driven environment. The culture emphasizes collaboration across regulatory, device development, quality, clinical, and human factors teams.

• Oversee the Complex Clinical Bill Review team, managing production expectations, SLAs, client communication, and team performance.
• Analyze and track internal business requirements, continuously evaluate functionality across programs, and perform requirements gathering to solve process issues.
• Monitor team performance metrics, identify growth opportunities, and coordinate system enhancements including JIRA and UAT testing.

Machinify is a leading healthcare intelligence company providing an AI-powered platform for health plan clients. They are deployed by over 85 health plans, representing more than 270 million lives, with a culture of innovation and efficiency.

• Provide procedural support to new users to promote safety and effective progression through their learning curves.
• Work with senior hospital staff and key physicians to integrate Ion at new customer sites, ensuring ongoing commitment and utilization.
• Facilitate critical user and procedural data capture to create effective benchmark metrics.

Intuitive is a global leader in robotic-assisted surgery and minimally invasive care, developing technologies like the da Vinci surgical system and Ion. With a team of engineers, clinicians, and innovators, the company fosters a culture of creativity, rigor, and collaboration to improve surgical outcomes.

• Manage and monitor soft tissue ablation clinical trials, including site start-up, patient recruitment, and data quality.
• Prepare study documents, oversee monitoring visits, and ensure compliance with FDA and ICH-GCP regulations.
• Mentor other CRAs and support both U.S.-based and future international clinical studies.

Pulse Biosciences is a novel bioelectric medicine company developing the CellFX nsPFA technology for non-thermal ablation. The company is publicly traded (Nasdaq: PLSE), fosters a culture of innovation and collaboration, and is committed to hiring top talent.

• Assists sales representatives with surgeon trainings, hospital robotic development, and territory management.
• Guides technical in-services for customers including OR staff and surgeons.
• Sells benefits of advanced technology to existing robotic users to contribute to team quotas.

Intuitive is a global leader in robotic-assisted surgery and minimally invasive care, known for the da Vinci surgical system and Ion. It is a large company with a team of engineers, clinicians, and innovators united by making surgery smarter, safer, and more human.

• Work with the Clinical Sales Manager to develop strategy for da Vinci system utilization and drive adoption.
• Become an expert in da Vinci surgery across specialties to support surgical robotics program development.
• Support field efforts to achieve quarterly sales goals and manage administrative tasks including reporting.

Intuitive is a pioneer in robotic-assisted surgery, developing the da Vinci Surgical System to expand physician capabilities. With over 25 years of industry leadership, the company fosters an inclusive culture and empowers team members from diverse backgrounds to make a difference.

• Lead and develop a world-class Service & Repair Quality organization across multiple international sites, driving continuous improvement and regulatory compliance.
• Apply global regulatory requirements to Service & Repair processes, including FDA, GMP, CAPA, ISO 13485, and lead quality support during regulatory inspections.
• Develop statistically sound sampling plans, use data analysis to identify trends, and build strong partnerships with site leadership and stakeholders.

This is a senior quality leadership opportunity within a global medical technology environment focused on delivering safe, reliable, and innovative healthcare solutions. The company is a partner of Jobgether, with operations across the US, Germany, and Japan, and emphasizes a collaborative, ethical, and inclusive culture.

• Manage provider credentialing, licensing, and payer enrollment activities from application through completion.
• Research and resolve non-routine credentialing and provider data discrepancies, ensuring compliance.
• Maintain accurate provider records, monitor deadlines, and communicate with stakeholders to prevent delays.

The company is a partner organization that manages hiring for healthcare credentialing roles. They operate remotely and foster a collaborative, deadline-driven culture focused on compliance and operational excellence.

• Support clinical process improvement initiatives and monitor performance to client SLAs.
• Conduct root cause analyses and develop remediation plans for process variations.
• Collaborate with product and analytics teams to optimize letters and template tracking.

Cohere Health’s clinical intelligence platform and agentic AI-powered solutions connect health plans and providers to optimize care quality and reduce costs. The company has been named to the Inc. 5000 list and ranked a Top 5 LinkedIn Startup, backed by leading investors, with a culture that values empathy and collaboration.

• Oversee all nursing activities for clinical research studies in the Southeast region, ensuring compliance with regulations and protocols.
• Manage per diem mobile research nurses, including training, documentation, and quality control of data collection.
• Serve as the nursing subject matter expert for assigned studies, collaborating cross-functionally to support study execution.

Science 37 accelerates clinical research by enabling universal trial access for patients through Direct-to-Patient Site and Patient Recruitment solutions, powered by a proprietary technology stack. The company employs in-house medical and operational experts to enhance quality and streamline study orchestration, fostering a culture of innovation and teamwork.