Trabajos clinical lab en San Diego, California - Page 3Crear alertas

Receive incoming lab orders and requisitions and enter relevant clinical data into the necessary software applications.

Voca Healthcare is seeking a travel Clinical Lab Scientist (CLS) for a travel job in San Diego, California. As a Voca Traveler, you will gain new clinical skills, visit amazing places and meet awesome healthcare professionals.

SHS staff consists of a diverse team of physicians, nurse practitioners, registered nurses, social workers, pharmacists, x-ray technologists, clinical laboratory scientists, medical lab assistants, optometrists, medical assistants, health educators, administrative and other healthcare professionals.

California Clinical Laboratory Scientist (CLS) Generalist license. Talent4Health is seeking a travel Clinical Lab Scientist (CLS) for a travel job in San Diego, California.

Job Description Job Title: Veterinary Research Scientist Primary Responsibilities: This position requires a broad knowledge of the anatomy and physiology of small and large animals to help develop and support in vivo models to screen therapeutics and devices being developed for various disorders. Experience with surgical, dosing and sampling techniques is required. In addition, the Veterinary Scientist is responsible for assisting in the clinical care of animals on surgical studies including post-operative monitoring and evaluations. Principal Duties and Responsibilities * Perform surgical support and provide anesthesia, surgical, and analgesic technical expertise/advice to facilitate protocol development. * Provide clinical and technical support to internal and external customers, regarding surgical models and services. * Serve as the Research Lead or Study Director responsible for preclinical studies in various species. * Assist in the preparation and review of study protocols and reports. * Provide support for activities of the Institutional Animal Care and Use Committee (IACUC), including protocol review, program review, and facility inspections. * Assist in activities to ensure the facility is in compliance with all applicable regulations, guidelines, and standards that relate to animal care and use. (USDA, FDA, and AALAC) * Train staff on in-vivo procedures * Make recommendations and assist in establishing and enhancing veterinary and animal care standards * Will administer controlled substances and be responsible for maintaining appropriate records. * May develop new or innovative surgical techniques or other procedural improvements appropriate to research studies. * Perform special projects and assist with administrative efforts as needed. Candidate Requirements: * Background in lab animal (in vivo) research with a focus on surgical techniques is a must. * Ability to perform study duties and responsibilities in multiple species with minimal supervision. * Must be flexible to work various schedules and hours as well as provide comprehensive, after hours, and on-call coverage as needed. * This position requires good communication skills and attention to detail. * Strong work ethic, self-motivation, and the ability to adapt to a dynamic team/work environment are keys to success. Education: * Degree in veterinary medicine (BVM, DVM, or VMD) preferred. * Graduate-level degree (M.S. or Ph.D.) in pharmaceutical science, life sciences, or pharmacology considered. Experience: * Minimum 5-7 years of relevant industry experience depending on education level. * Experience working with both small and large animals preferred. * Working knowledge of imaging modalities (TEE, C-arm) will be a plus * A comprehensive understanding of the requirements for GLP study execution and documentation is required.

Must have current Clinical Laboratory Scientist issued by the State of California, Department of Public Health. Two (2) years of applicable clinical laboratory experience. Six (6) years of applicable clinical laboratory experience.

Job DescriptionTitle: Medical assistants Location: La Jolla, CA (onsite)Office Hours: • Monday/Tuesday/Wednesday/Thursday: 8:30am-4:30pm, • Friday: 8:30am-1:30pm Position: Full Time – hourly payOvertime: YesQuantity: Two (2)Job Summary:Help with patient intake, room patients, assist doctors with clinical duties, procedures, follow up lab results, manage patient prescription requests, back-office duties. Requirements:, • OB/GYN practice experience is required, • Years of experience, • Education, • Technical skills

Staff consists of physicians, psychiatrists, psychologist, pharmacists, optometrists, nurse practitioners, registered nurses, social workers, radiology technologists, clinical laboratory scientists, medical lab assistants, medical assistants, health educators, administrative and other healthcare pro

Clinical Lab Supervisor - Rapid Response Lab. California Clinical Laboratory Scientist License. Demonstrated ability to apply principles in a clinical laboratory setting.

Clinical Laboratory Scientist (CLS) or appropriate sub-specialty license issued by the State of California, Department of Public Health. Other responsibilities include method development-modification-parallel testing, collaboration on or preparation of abstracts or manuscripts, repair of laboratory

Other responsibilities include method development-modification-parallel testing, collaboration on or preparation of abstracts or manuscripts, repair of laboratory instruments, sample processing, reagent preparation, data entry and phlebotomy duties. All Clinical Laboratory Scientists may process spe

Job Description About the Role: Do you have a passion for helping people see clearly and look their best? We’re seeking an Eyewear Specialist to provide exceptional patient care while guiding frame and lens selections. This role combines technical expertise with customer service, giving you the chance to make a direct impact on patients’ daily lives. Core Responsibilities: • Assist patients in selecting frames and lenses tailored to their lifestyle, comfort, and visual needs., • Educate patients on lens options, coatings, sunglasses, and specialty solutions to enhance their experience., • Take accurate measurements and ensure proper fit for all lens types, including single vision, bifocal, and progressive lenses., • Promote the benefits of owning multiple pairs of glasses for work, recreation, and daily life., • Verify insurance coverage and clearly explain benefits to patients., • Dispense eyewear, provide guidance on prescription adaptation, and support lens performance., • Perform minor adjustments, repairs, and ongoing eyewear support as needed., • Respond promptly to patient calls and provide updates on order status., • Support day-to-day office operations and assist with other tasks as necessary., • Preferred: experience with edging, finishing, or surfacing in an optical lab. Key Competencies: • Customer Focus: Deliver a high-touch, patient-centered experience that exceeds expectations., • Sales & Consultative Approach: Build rapport, educate patients, and guide product selections that drive practice growth., • Collaboration: Work seamlessly with colleagues, supervisors, and managers to maintain smooth clinic operations., • Technical & Software Skills: Proficient with Excel, Word, email, inventory/order processing, payroll systems, and basic project management tools., • Communication: Strong verbal and written skills; comfortable presenting to patients and documenting routine reports., • Optical Knowledge: Prior optical experience is preferred and highly valued., • Flexibility & Cross-Training: Willing to learn other roles and adapt to evolving needs in a fast-paced environment. Why You’ll Love Working Here: • Directly impact patients’ quality of life and vision health., • Join a collaborative team that encourages learning and professional growth., • Gain hands-on clinical exposure with real opportunities for advancement in the optical field. Ready to Apply? If you’re passionate about optics, enjoy working with people, and want to grow in a dynamic clinical environment, we want to hear from you! Company DescriptionWe're not just a staffing company - we're a people company. At Amtec, we care about helping you reach your unique career goals. Since 1959, we’ve changed the lives of thousands of people for the better - people just like you. It’s our purpose to help you find meaningful work by matching your character, competence, and culture with an organization that truly values what you have to offer.We're not just a staffing company - we're a people company. At Amtec, we care about helping you reach your unique career goals. Since 1959, we’ve changed the lives of thousands of people for the better - people just like you. It’s our purpose to help you find meaningful work by matching your character, competence, and culture with an organization that truly values what you have to offer.

Job DescriptionSalary: About Artiva: Artiva is clinical-stage, publicly-traded biotechnology company focused on developing natural killer (NK) cell-based therapies for patients suffering from devastating autoimmune diseases and cancers. Artivas lead program, AlloNK, is an allogeneic, off-the-shelf, non-genetically modified NK cell therapy candidate designed to enhance the antibody-dependent cellular cytotoxicity effect of monoclonal antibodies to drive B-cell depletion. AlloNK is delivered in the outpatient setting with no required hospitalization. AlloNK is currently being evaluated in three ongoing clinical trials for the treatment of B-cell driven autoimmune diseases. This includes two company-sponsored trials, one in systemic lupus erythematosus for patients with or without lupus nephritis, and a basket trial across autoimmune diseases (Rheumatoid Arthritis, Systemic Sclerosis, Idiopathic Inflammatory Myopathies and Sjgrens Disease), as well as an investigator-initiated basket trial in B-cell driven autoimmune diseases. Artivas pipeline also includes CAR-NK candidates targeting both solid and hematologic cancers. Artiva was founded in 2019 as a spin out of GC Cell, formerly GC Lab Cell Corporation, a leading healthcare company in the Republic of Korea, pursuant to a strategic partnership granting Artiva exclusive worldwide rights (excluding Asia, Australia and New Zealand) to GC Cells NK cell manufacturing technology and programs. Artiva is headquartered in San Diego, California. For more information, visit. Job Summary: This position is responsible for cGMP auditing and supplier management activities at Artiva. Duties/Responsibilities: • Perform GMP/GDP audits in accordance with the external and internal audit program., • Support GXP audits (GLP, GCP, GCLP), as necessary., • Perform Drop-In GMP Internal audits., • Create and maintain audit schedules., • Track audit responses to completion., • Oversee and maintain the supplier qualification program., • Support the creation and execution of Quality Agreements with suppliers., • Update databases, prepare metrics, identify and communicate trending and tracking of audits and related supplier management activities., • Support audits by regulatory or state agencies and partners., • Support QA review of Analytical Development and Process Development data and reports, as needed., • Follow applicable regulations, including FDA, ISO, ICH, company policies and procedures., • Support other QA department needs as identified by management. Requirements: • Bachelors degree or a combination of relevant education and applicable job experience, • 5+ years experience in an FDA regulated industry and expert knowledge of CGMP regulations, • Certified Quality Auditor credential is a plus., • Ability to adapt quickly to shifting needs and/or priorities, • Able to interface well with all levels of personnel, • Excellent communications skills, both written and verbal and a high degree of professionalism, • Exceptional attention to detail, • Flexibility to travel Why you should apply: We have a fantastic team and philosophy! We are passionate we deeply care about our team, our science, and improving the lives of patients. We are tenacious laser-focused on our mission and undeterred in our commitment to deliver life-saving medicines for cancer patients.We are innovative - pushing into new frontiers for patient benefit.We are transparent - believers in flat, accessible, and open communication paths.We are inclusive committed to the diversity of our team and ensuring that all voices are heard. In addition to a great culture, we offer: A beautiful facility An entrepreneurial, highly collaborative, and innovative environment Comprehensive benefits, including: • Medical, Dental, and Vision, • Group Life Insurance, • Long Term Disability (LTD), • 401(k) Retirement Plan with match, • Employee Assistance Program (EAP), • Flexible Spending Account (FSA), • Paid Time Off (PTO), • Company paid holidays, including the year-end holiday week Base Salary: $100,000 - 120,000.Exact compensation may vary based on skills and experience.

Job DescriptionSalary: $60-65/hr Join one of Southern Californias most trusted vein and vascular centers! La Jolla Vein Care is currently seeking a skilled and experienced Vascular Technologist (RVT or RVS) to join our team in La Jolla, CA on a part-time, 1099 contract basis (24 days/week). About Us: La Jolla Vein Care is a leading, IAC-accredited vein and vascular center, recognized for excellence in patient care and vascular diagnostics. We specialize in comprehensive vein treatments and diagnostic ultrasound services, with a strong commitment to innovation, quality, and patient experience. Position Highlights: • Schedule: Exact days per week, TBD, will fall on a week day MondayFriday (no weekends, nights, or on-call!), • Compensation: $60$65 per hour (contract/per diem) Depends on vein clinic/ vascular lab experience, • Hours: 1632 hours per week (flexible), • Work type: 1099 Independent Contractor, • Perform venous insufficiency studies, DVT studies, and vein mapping, • Generate preliminary reports via our cloud-based PACS system, • Relay abnormal results to the reading or referring physician, • Educate patients and explain procedures with professionalism and clarity, • Maintain a clean and compliant work area following IACprotocols, • Collaborate with the clinical team to deliver high-quality care, • Perform ABIs Preferred Qualifications: • 2+ years of experience performing vascular ultrasound, including reflux studies, • Proficient in imaging patients in standing and reverse Trendelenburg positions, • Strong skills in DVT studies and vein mapping, • Knowledge of endovenous procedures such as RFA, sclerotherapy, and phlebectomy is a plus, • Graduate of an accredited ultrasound program (vascular-focused preferred), • Credentialed: RVT (ARDMS) or RVS (CCI), • No nights, weekends, or on-call shifts, • Flexible, supportive work environment, • Learn new skills and expand your vascular imaging expertise, • Part-Time, • Contract (1099)

Job DescriptionSalary: About Artiva: Artiva is clinical-stage, publicly-traded biotechnology company focused on developing natural killer (NK) cell-based therapies for patients suffering from devastating autoimmune diseases and cancers. Artivas lead program, AlloNK, is an allogeneic, off-the-shelf, non-genetically modified NK cell therapy candidate designed to enhance the antibody-dependent cellular cytotoxicity effect of monoclonal antibodies to drive B-cell depletion. AlloNK is delivered in the outpatient setting with no required hospitalization. AlloNK is currently being evaluated in three ongoing clinical trials for the treatment of B-cell driven autoimmune diseases. This includes two company-sponsored trials, one in systemic lupus erythematosus for patients with or without lupus nephritis, and a basket trial across autoimmune diseases (Rheumatoid Arthritis, Systemic Sclerosis, Idiopathic Inflammatory Myopathies and Sjgrens Disease), as well as an investigator-initiated basket trial in B-cell driven autoimmune diseases. Artivas pipeline also includes CAR-NK candidates targeting both solid and hematologic cancers. Artiva was founded in 2019 as a spin out of GC Cell, formerly GC Lab Cell Corporation, a leading healthcare company in the Republic of Korea, pursuant to a strategic partnership granting Artiva exclusive worldwide rights (excluding Asia, Australia and New Zealand) to GC Cells NK cell manufacturing technology and programs. Artiva is headquartered in San Diego, California. For more information, visit. Job Summary: The Senior Director of Regulatory Affairs is responsible for primary authorship and supporting regulatory activities, preparing regulatory submissions and ensuring compliance with global regulatory requirements. The ideal candidate will have a strong background in cell and gene-modified cell therapy, expertise in global regulatory requirements, and preferably late-stage development experience. Duties/Responsibilities: • Support the preparation, review, and submission of regulatory filings, including INDs, CTAs, BLAs, and MAAs, ensuring compliance with global regulatory requirements., • Assist in compiling and organizing regulatory documents and responding to health authority queries., • Work closely with cross-functional teams, including Clinical, Pharmacovigilance, Biometrics, and CMC, to ensure accurate and complete regulatory submissions., • Maintain up-to-date knowledge of global regulatory requirements and contribute to regulatory intelligence efforts., • Support regulatory interactions with global health authorities by preparing meeting materials and responses to requests., • Contribute to the development of regulatory documentation, including CTD dossiers, IBs, clinical protocols, nonclinical and clinical study reports., • Assist in tracking regulatory commitments and timelines to ensure timely submissions and approvals., • Provide hands-on support in assessing emergent clinical data and operational activities for regulatory compliance. Professional Experience/Qualifications: • Bachelors degree required; advanced degree preferred., • 10+ years experience in a fast-paced, high-volume document production environment (e.g., documentation, publications, formal meetings) with at least 5 in the cell and gene therapy space., • Strong knowledge of regulations and guidelines across multiple global jurisdictions, including the U.S., EU, and other key regulatory agencies., • Hands-on experience in the preparation and submission of regulatory filings (e.g., INDs, CTAs, BLAs, and MAAs)., • Strong organizational skills and attention to detail, with the ability to manage multiple priorities effectively., • Excellent written and verbal communication and collaboration skills to work effectively with cross-functional teams., • Ability to thrive in a fast-paced environment and adapt to changing regulatory requirements. Why you should apply: We have a fantastic team and philosophy! We are passionate we deeply care about our team, our science, and improving the lives of cancer patients. We are tenacious laser-focused on our mission and undeterred in our commitment to deliver life-saving medicines for cancer patients.We are innovative - pushing into new frontiers for patient benefit.We are transparent - believers in flat, accessible, and open communication paths.We are inclusive committed to the diversity of our team and ensuring that all voices are heard. In addition to a great culture, we offer: A beautiful facility An entrepreneurial, highly collaborative, and innovative environment Comprehensive benefits, including: • Medical, Dental, and Vision, • Group Life Insurance, • Long Term Disability (LTD), • 401(k) Retirement Plan, • Employee Assistance Program (EAP), • Flexible Spending Account (FSA), • Paid Time Off (PTO), • Company paid holidays, including the year-end holiday week, • Our recognition program, Bonus.ly, is where you can trade in points earned for things you want. If all this speaks to you, come join us on our journey! Base Salary: $240,000 - $260,000. Exact compensation may vary based on skills and experience.

Job DescriptionPart time Clinical Intake Specialist position available for qualified applicant that will assist Intake Specialist with referrals, calling Case Managers, Discharge Planners and Physician's offices to obtain orders, H&P's and demographics for new and recertified patients. Order DME, Audit Patient Profiles for accuracy, report lab results to physician and RN's. Currently a part time position,will turn into full time. Hours availability needed are:Monday 8:00-12:00Tuesdays 12:30-4:30Wednesdays 8:00-4:30Thursday 12:30-4:30 You can work as a Home Health LVN per visit if interested in working additional hours till full time available.Home Health experience required with a minimum of 2 years nursing experience. Great opportunity for those interested in working administratively. Must have good verbal and communication skills, organizational/planning skills. Able to manage multiple tasks simultaneously and ability to maintain confidentiality. Knowledge of computing hardware and software resources including web activity. Please reply to this job posting with an attached resume Always Best Care Assisting Clinical Manager to keep all records up to date and accurate. Responsibilities:* calling Case Managers, Discharge Planners and Physician's offices to obtain orders, H&P's and demographics for new and recertified patients. Order DME, Audit Patient Profiles for accuracy, report lab results to physician and RN's. Qualifications:* LVN or RN License

Travel Laboratory: Clinical Laboratory Scientist San Diego, CA. Travel Clinical Lab Scientist Allied. Specialty: Clinical Lab Scientist Allied.

Travel Laboratory: Clinical Laboratory Scientist San Diego, CA. Travel Clinical Lab Scientist Allied. Specialty: Clinical Lab Scientist Allied.

Medical & Business Info Systems Administrator. Staff consists of physicians, psychiatrists, psychologist, pharmacists, optometrists, nurse practitioners, registered nurses, social workers, radiology technologists, clinical laboratory scientists, medical lab assistants, medical assistants, health edu

Must have a current Clinical Laboratory Scientist (CLS) or appropriate sub-specialty license issued by the State of California, Department of Public Health. At least two years of applicable clinical laboratory experience. The Clinical Lab Scientist position is compensated at $56.

Fusion Medical Staffing-Laboratory is seeking a travel Clinical Lab Scientist (CLS) for a travel job in San Diego, California. Fusion Medical Staffing - Laboratory Job ID #1837759. About Fusion Medical Staffing-Laboratory.

CLS) Clinical Lab Scientist Specialist, Per Diem. Current Clinical Laboratory Scientist or appropriate subspecialty license issued by the State of California Department of Public Health. Applicable clinical laboratory experience.

Are you an experienced Clinical Lab Professional? If so, Labcorp wants to speak with you about exciting opportunities to join our team as a Medical Lab Technician in the Urinalysis Department of Labcorp located in San Diego CA.

Triage Staffing is seeking a travel nurse RN Float ICU - Intensive Care Unit Med Surg for a travel nursing job in San Diego, California. • Specialty: ICU - Intensive Care Unit, • Discipline: RN, • Start Date: 12/08/2025, • Duration: 13 weeks, • 36 hours per week, • Shift: 12 hours, nights Apply for specific facility details.ICU RN Triage Staffing Job ID #AWWHWH9D. Posted job title: Nursing: Intensive Care Unit At Triage, we prefer to be real. Real about expectations—both ours and yours. Real about how a decision you make today could affect your tomorrows. Real about how compensation actually works. Real about how great—or grating—your next supervisor may be. Being real allows everyone at Triage to be ready. Ready to serve you with real honesty. So if that gig near the ocean is really no day at the beach, or that third shift comes with a second-class rate, we tell you. So you can be ready, too. We staff all five major divisions of acute care—nursing, lab, radiology, cardiopulmonary and rehab therapy, offering: • Competitive, custom pay packages, • One point of contact for both travelers and facilities (per division), • A reliable recruiter who's got your back throughout your entire assignment, • In-house compliance and accounting specialists, • A clinical liaison team available 24/7 to offer medical and professional support and career development, • A mentoring program that is run and managed by actual clinicians—yeah, you read that right, • And more (because of course there’s more) Are we the biggest? No. Are we the best? That’s rather subjective, but we’re trying to be. Will we work like hell to get you as close to your idea of heaven as possible? Yes. Yes, we will. Benefits: • Day One comprehensive, nationwide insurance plans for health, vision and dental and life—including a HSA option, • Day One 401(k) program with employer-matching contributions once eligible, • Facility cancelling protection—your time is money on and off-the-clock, • Guaranteed hours, • Weekly paychecks via direct deposit, • Earned vacation bonuses for time worked, • Paid holidays, • Employee assistance program (EAP)—your mental health is important, too, • Continuing education, certification and licensing reimbursement, • Workers comp—because accidents happen, • Top-rated professional liability insurance, • Company provided housing options, • Referral bonus—$750 in your pocket after they’ve completed a 13-week assignment

Bachelor's degree in a chemical, biological, physical, or clinical lab science (or qualifying equivalent).

Job DescriptionDescription: Onsite | San Diego, CA Our medical device client is seeking a hands-on IT Lab Specialist who thrives in technical environments and enjoys solving complex challenges. In this role, you’ll manage lab operations, set up hardware/software systems, and work closely with IT and engineering teams to keep everything running seamlessly. Due to client requirement, applicants must be willing and able to work on a w2 basis. For our w2 consultants, we offer a great benefits package that includes Medical, Dental, and Vision benefits, 401k with company matching, and life insurance. Rate: $45 - $50 / hr. w2 Responsibilities: • Be the go-to person for lab maintenance and support., • Configure Mac and PC systems with standardized images and security patches., • Work with IT to ensure seamless network connectivity., • Assemble racks, servers, and update hardware for validation., • Build and manage virtual machines to scale test infrastructure., • Procure and track test equipment and inventory., • Install automation tools for monitoring and data collection., • Document lab layout, processes, and device info for easy access., • Lab Management experience., • Scripting skills (Python or Shell)., • QA automation experience., • Development background., • Bachelor’s degree in Computer Science, IT, or related field., • 3–5 years in lab management or IT infrastructure support, • Familiarity with virtualization and automation tools., • Certifications like CompTIA A+, Network+, Python, or VMware are a plus. Skills, experience, and other compensable factors will be considered when determining pay rate. The pay range provided in this posting reflects a W2 hourly rate; other employment options may be available that may result in pay outside of the provided range. W2 employees of Eliassen Group who are regularly scheduled to work 30 or more hours per week are eligible for the following benefits: medical (choice of 3 plans), dental, vision, pre-tax accounts, other voluntary benefits including life and disability insurance, 401(k) with match, and sick time if required by law in the worked-in state/locality. Please be advised- If anyone reaches out to you about an open position connected with Eliassen Group, please confirm that they have an Eliassen.com email address and never provide personal or financial information to anyone who is not clearly associated with Eliassen Group. If you have any indication of fraudulent activity, please contact . About Eliassen Group: Eliassen Group is a leading strategic consulting company for human-powered solutions. For over 30 years, Eliassen has helped thousands of companies reach further and achieve more with their technology solutions, financial, risk & compliance, and advisory solutions, and clinical solutions. With offices from coast to coast and throughout Europe, Eliassen provides a local community presence, balanced with international reach. Eliassen Group strives to positively impact the lives of their employees, clients, consultants, and the communities in which they operate. Eliassen Group is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, pregnancy, sexual orientation, gender identity, national origin, age, protected veteran status, or disability status. Don’t miss out on our referral program! If we hire a candidate that you refer us to then you can be eligible for a $1,000 referral check!

Job Description Job title Care Coordinator – Accelerated Cancer Screening Reports to Health Navigator Supervisor, Medical Director Status Full-Time (1 Year Grant Funded Position) Salary$22.00 - $24.00 OPSAM HEALTH MISSION We exist to provide quality and patient-centered healthcare to every member of the communities we serve, regardless of the ability to pay. OPSAM Health is a Federally Qualified Health Center (FQHC) that serves the San Diego County community. Founded in 1973 in a barber shop in Downtown San Diego by Filipino health professionals offering services to immigrants who did not have the finances, linguistic skills, or ability to navigate the health care system. Today, Operation Samahan has evolved into a diverse community health center with services available in National City, Mira Mesa, City Heights, and Rancho Penasquitos. We provide primary care, dental, behavioral health, family planning, integrative health and wellness, healthy eating, civic engagement, and other health-related services to the uninsured, underinsured, and underserved families of all income levels, regardless of their ability to pay. JOB PURPOSE The Care Coordinator - Accelerated Cancer Screening will focus on closing cancer screening care gaps for Opsam Health patients, ensuring timely follow-up for abnormal breast, cervical, and colorectal screenings. They will collaborate with clinical teams to guide patients through each step of the screening and follow-up process, addressing any barriers to care. This role includes managing referrals, coordinating with external providers, and auditing patient records to ensure quality care. Additionally, the coordinator will work with the Quality Improvement team to enhance educational and training efforts related to cancer screening’s ESSENTIAL DUTIES AND RESPONSIBILITIES • Responsible for reducing cancer screening care gaps for Opsam Health patients, • Oversee clinic care coordinator's daily huddle regarding cancer prevention screening efforts, • Support to clinicians to navigate patients through each step in the process of any abnormal breast, cervical and colorectal cancer screening results, assisting patients in accessing recommended follow-up care, including additional imaging, tests and appointments at tertiary care centers, • Ensure proper communication with patients, clinical staff, providers, lab and imaging partners to assure the patients’ timely and appropriate care, • Audit chart records in eClinicalWorks for cancer screening and follow up reports, • Assist patients with referrals related to breast, cervical and colorectal abnormalities, • Schedule appointments/ referrals with appropriate provider(s) for cervical, breast and colon cancer screening diagnosis, and treatment, including contacting and reminding patients to schedule appointments, anticipatory guidance about expected tests and procedures, and navigate on how to arrive at scheduled appointments on time and prepared, • Request medical records from outside care providers and upload to ensure accurate and complete medical record, • Consider and strategically address the “social determinants of health” which may be delay or otherwise interfere with timely and appropriate follow-up services, • Collaborate with QI Team in the planning and implementation of educational, training and quality improvement efforts for cancer screening, • Coordinate all newly diagnosed cancer to oncology specialists (such as Moore’s Cancer Center) to ensure timely evaluation and management, • Other duties assigned as needed Qualifications • Medical Assistant, Bachelor’s degree in healthcare field or High School Diploma with at least 2 years of clinical care coordination experience., • Knowledge of medical terminologies, • Experience working in a large clinic setting, • Experience working with Health Insurance plans, • Knowledge of scheduling medical appointments and prior authorization processes., • Experience with electronic medical records, • Excellent ability to communicate both orally and in writing., • Demonstrated knowledge and advanced level skill in word processing software applications (Word, Excel, Teams, Outlook, & PowerPoint), • Ability to interact well with care teams and all patients and families., • Excellent customer service skills.

Job Description The Field Procedural Specialist (FPS) is responsible for providing technical, clinical, and educational expertise to ensure safe product use while supporting implants and ongoing follow-up visits during the Global Pivotal Study (GPS). The FPS will report to the Manager, Field Procedural Specialist Group within the Clinical Studies Department, interacting with the Leadless Pacemaker Global Training Manager during the Global Pivotal Study and through commercialization. RESPONSIBILITIES: Training • Provide clinical expertise at the company training labs, including hands on implant procedure training with several physicians at a time in a simulated EP lab setting., • Assist in onsite education and technical training activities with physicians and hospital support staff., • Educate implanting teams on proper indications for use of the Leadless Pacemaker procedures., • Provide support on questions regarding device follow up and programming., • Facilitate onsite training in-service with staff on procedure simulators, including simulated procedures and procedural troubleshooting., • Responsible for implant and follow-up visit procedure, support in compliance with the instructions for use and trial protocol., • Carry products and work with clinical studies team to manage site inventory to ensure adequate product at clinical study site., • Collaborate and partner with the local Field Clinical Studies Engineering team responsible for protocol execution., • Assist the clinical studies team in data collection during implant and follow-up visits to support protocol requirements., • Responsible for scheduling individual travel arrangements to ensure site implant and follow-up coverage, with potential for site coverage for emergent checks or at times in other areas of the country., • Maintains a high level of communication with study sites and customers, Manager, FPS Group, and the GPS study team, including the Field Clinical Studies Engineering group, throughout the Global Pivotal Study., • FPS and FCSE are expected at implant/ follow-up with FPS focus on implant procedure support and programming and FCSE focus on study protocol requirements, • Professional written and verbal communication skills., • Provide updates to management to help improve the technology for next generation designs., • Working with the program coordinator to ensure coverage., • Submit accurate and timely expense reports. QUALIFICATIONS: • Bachelor's degree in engineering, biological sciences, or a related field, OR equivalent or related experience in cardiology or clinical research., • 3+ years sales and/or cardiac device technical experience in a hospital environment selling or supporting cardiac electrophysiology or cardiovascular implantable product., • Prior experience with Cardiac Rhythm Management required, with a strong preference of prior leadless pacemaker experience., • Preference for CCDS certification., • 75% overnight travel may be required.