Title: Senior Clinical Research Coordinator Location: San Diego, California Job Description: At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion. Artemis Research is a leading principal investigator- and patient-focused clinical research company dedicated to advancing medical treatments. Established in 2008 by colleagues who bring more than 50 years of combined research experience, Artemis specializes in Psychiatry/Neurology, Internal Medicine, and Women’s Health studies. With multiple locations serving Southern California, including San Diego and Riverside, each Artemis site is fully equipped to conduct complex clinical research trials. Together with Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion. Want to be a part of a growing company that’s making a difference in our world? Look no further than Artemis Institute for Clinical Research! You’ll enjoy a friendly and exciting culture with opportunities for growth and advancement. We offer the following generous benefits to our full-time employees: - A range of PPO and HMO medical plans - PPO and HMO dental plans - Vision coverage, long term disability plan, and life/AD&D coverage - 401k plan - Paid holidays and paid time off - A welcoming work environment We’re looking for a bright, talented new team member to be a part of our story. Check out this current opening and if you think you may be a fit for the role, please apply. The Role Artemis is looking for a Senior Clinical Research Coordinator for the San Diego office. Under the supervision of the Site Director, the Senior Clinical Research Coordinator is responsible for the conduct of research protocols, such that the integrity and quality of the clinical research is maintained and the research is conducted in accordance with Good Clinical Practice Guidelines. The Sr. Clinical Research Coordinator manages study conduct from planning through study closeout. Type: Regular Full-time Employee Location: Onsite in San Diego, CA (no capabilities for remote or hybrid work) Reports to: Site Director Pay: $70,304-75,000/yr, dependent upon years of experience, licenses and certifications, and education pertinent to the role. Work Schedule: Monday & Thursday - 8:30am-5pm / Tuesday, Wednesday, and Friday 7:00am-3:30 pm Responsibilities: - In-depth understanding of Pharmaceutical Sponsor/Industry initiated FDA studies in order to conduct the study with excellent quality - Managing all aspects of a study including participating in the informed consent process, coordinating and performing all visit study procedures per the protocol, entering data and query resolution, Investigational Product management, and managing all study related supplies and equipment, hosting monitoring visits, and attending Investigator Meetings - Providing the highest level of care for study patients and delivering excellent customer service to the Pharmaceutical clients - Assist with lab draws, processing and shipping - Some supervision of direct reports may be required - Duties, responsibilities, and activities may change or new ones may be assigned at any time with or without notice Requirements: - Bachelors Degree preferred - Minimum five plus (5+) years of experience as a Clinical Research Coordinator required - Experience supervising other employees strongly preferred - Medical assistant or phlebotomist required - Commitment and ability to deliver excellent customer service - Excellent communication, punctual and responsible - Extremely well organized - Excellent verbal and written communication skills - Trustworthy, reliable; attentive to details - Mature and pleasant demeanor - Willingness to learn new tasks and grow with the company

Title: Senior Clinical Review Nurse - Prior Authorization Location: Remote-NY Full time Job Description: You could be the one who changes everything for our 28 million members as a clinical professional on our Medical Management/Health Services team. Centene is a diversified, national organization offering competitive benefits including a fresh perspective on workplace flexibility. This position requires NY State Licensure as a RN, OT or PT Position Purpose: Routinely reviews more challenging prior authorization requests to determine medical necessity of service and appropriate level of care in accordance with national standards, contractual requirements, and a member's benefit coverage. Assesses more complex authorization requests and provides recommendations to the appropriate medical team to promote quality and cost effectiveness of medical care. - Performs medical necessity and clinical reviews of authorization requests to determine medical appropriateness of care in accordance with regulatory guidelines and criteria - Collaborates with healthcare providers and authorization team to ensure timely review of services and/or requests to ensure members receive authorized care - Escalates prior authorization requests to Medical Directors as appropriate to determine appropriateness of care - Manages service authorization requests for a member’s transfer or discharge plans to ensure a timely discharge between levels of care and facilities - Provides feedback on opportunities to improve the authorization review process for members - Manages as appropriate with healthcare providers, utilization management team, and care management team to assess medical necessity of care - Partners with interdepartmental teams on projects within utilization management as part of the clinical review team - Manages and reviews all member’s clinical information in health management systems to ensure compliance with regulatory guidelines - Provides education to providers and/or interdepartmental teams on utilization processes to promote high quality and cost-effective medical care to members - Develops in-depth knowledge of the prior authorization process and acts as a trainer to other team members - Performs other duties as assigned - Complies with all policies and standards Education/Experience: Requires Graduate from an Accredited School of Nursing or Bachelor’s degree in Nursing and 4 – 6 years of related experience. Advanced clinical knowledge and ability to analyze authorization requests and determine medical necessity of service preferred. Strong knowledge of Medicare and Medicaid regulations preferred. Strong knowledge of utilization management processes preferred. License/Certification: - For Fidelis Plan Only: A clinical degree as a healthcare professional is required along with the appropriate license. Examples include Nursing, PT and OT. required Pay Range: $30.58 - $55.09 per hour Centene offers a comprehensive benefits package including: competitive pay, health insurance, 401K and stock purchase plans, tuition reimbursement, paid time off plus holidays, and a flexible approach to work with remote, hybrid, field or office work schedules. Actual pay will be adjusted based on an individual's skills, experience, education, and other job-related factors permitted by law, including full-time or part-time status. Total compensation may also include additional forms of incentives. Benefits may be subject to program eligibility. Centene is an equal opportunity employer that is committed to diversity, and values the ways in which we are different. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other characteristic protected by applicable law.

• The Clinical Genomics Scientist II analyzes clinical genetics data, curates variants and genes, and summarizes findings for clinical reports. • Assist laboratory directors and R&D with validation of cutting-edge technologies and software platforms. • Curation (50%): curation of variants, genes, and gene-disease correlation following ACMG guidelines. • Analysis (30%): analyzing clinical genomics data, selecting variants for curation/confirmation, variant nomenclature following HGVS guidelines. • Other (20%): may involve clinical report drafting, test validation, process refinement, presenting findings, monitoring test turnaround time and task delegation.

• The Clinical Genomics Scientist II analyzes clinical genetics data, curates variants and genes, and summarizes findings for clinical reports. • Our scientists assist laboratory directors and R&D with validation of cutting-edge technologies and software platforms. • Curation (50%): curation of variants, genes, and gene-disease correlation following ACMG guidelines. • Analysis (30%): analyzing clinical genomics data, selecting variants for curation/confirmation, variant nomenclature following HGVS guidelines. • Other (20%): may involve clinical report drafting, test validation, process refinement, presenting findings, monitoring test turnaround time and task delegation.