The Center for Sports Medicine and Orthopaedics is seeking an RN/LPN for a part-time position to triage patients remotely in Chattanooga, TN. Center for Sports Medicine & Orthopaedics is Chattanooga's leading provider of multi-specialty orthopaedic care since 1979. We have 12 convenient locations in the Chattanooga, North Georgia and surrounding area. We offer advanced sports medicine, orthopaedics, surgery, physical and occupational therapy and sports training. Benefits include 401(k)/401(k) matching, and paid time off. Current TN or GA multi-state nursing license required. BLS (CPR) certification preferred. Orthopaedic experience is a plus. Excellent customer service skills required. Schedule: Average 30 hours weekly, from 1:00 PM to 7:00 PM, including live phone queue coverage from 1:00 PM to 5:00 PM and after-hours answering service from 5:00 PM to 7:00 PM. No weekends/holidays.

About Affect Affect is transforming behavioral health care by combining mobile technology with counseling and medical services to deliver 100% virtual, evidence-based treatment. Our mission is to break down barriers to care—making treatment more accessible, engaging, and effective for our members. Through our innovative model, we integrate a smartphone app with a dedicated care team to provide real-time, data-driven support, improving outcomes while reducing costs. About the Role As a Psychiatric Mental Health Nurse Practitioner (PMHNP) at Affect, you’ll play a key role in leading member care alongside a collaborative team of counselors, therapists, peer support specialists, and case managers. You’ll provide evidence-based treatment for individuals navigating substance use and mental health disorders in a fully virtual environment. Affect specializes in substance-specific care. We prescribe Suboxone for Opioid Use Disorder and do not prescribe other controlled substances. While we provide extensive training in our treatment approach, clinical decisions remain at the provider’s discretion in collaboration with the member. For full-time roles, we are specifically seeking providers who are particularly strong on the mental health side. While experience with substance use disorder treatment and Suboxone prescribing is important, this role requires confidence in assessing and managing more complex mental health conditions. You must hold an active, unrestricted license in New Mexico. We are currently hiring for both full-time and part-time opportunities in New Mexico.This posting is for the full-time position ONLY. Key Responsibilities - Conduct initial and follow-up telehealth evaluations - Provide care for both substance use and mental health conditions - Prescribe medications as appropriate and respond to member questions - Complete timely documentation in our EHR (Healthie) - Collaborate with your care team and participate in scheduled team meetings Requirements - Active, unrestricted PMHNP license in New Mexico (Medicaid enrollment a plus) - Active license in your state of residence if different from New Mexico - Minimum of 2 years of experience (addiction or mental health preferred; strong candidates with less experience considered) - Experience prescribing Suboxone and an active DEA registration - Willingness to obtain additional state licenses (covered by Affect) - Strong empathy for individuals facing behavioral health challenges - Comfort using technology, including EHRs and mobile applications Additional Information This is a fully remote position. You’ll need a private, quiet workspace and reliable internet connection to conduct HIPAA-compliant telehealth visits. The role may include occasional internal meetings. Reasonable accommodations are available as needed. Why Join Affect? At Affect, we’re reimagining how behavioral health care is delivered. You’ll join a mission-driven, collaborative team focused on meaningful, outcomes-based care. We offer: - Competitive compensation - Fully remote flexibility - Opportunities for professional growth - A supportive, innovative culture If you’re passionate about making a real impact in behavioral health, we’d love to connect. Come be part of the Affect mission!!!

Location: Work from home (Pennsylvania) Shift: Days (United States of America) Scheduled Weekly Hours: 40 Worker Type: Regular Exemption Status: Yes Job Summary: Join our pharmacy team and practice at the top of license! The position includes a sign-on bonus for qualified candidates! Responsible for the management of patients being prescribed specialty medications by communicating with and supporting these patients and as well as developing and coordinating patient care within the clinical care team. This individual will coordinate the activities and lead resolution of issues between Pharmacy, provider and patient to ensure that all aspects of the patient care are clearly understood. Job Duties: - Support the overall CareSite Specialty Rx goals and objectives that result in improved quality of patient care and higher levels of patient satisfaction. - Assumes responsibility for the delivery of pharmaceutical care to patients by interpreting prescriptions, making necessary professional determinations regarding medications and various drug interactions, drug utilization review, generic substitution, and accurately filling and dispensing the prescription. - Provides drug and clinical information to other healthcare professionals in response to specific questions relating to issues pertinent to the care of patients. - Utilizing knowledge of medical practice, healthcare insurance procedures and pharmacy regulations, assists in clinical practice by helping patients gain better insight into their health conditions and how to comply with physicians’ instructions and advice and function as a conduit between the healthcare insurance company, physician’s office and the pharmacy. - Assists with the Prior Authorization and approval process and the statement of medical necessity. - Provide injection training and patient teaches as required. - Participate with community and regional patient advocacy and disease state support groups to educate and communicate the issues and opportunities within the Specialty Pharmacy Provider market. - Identifies patients at risk for therapy non-compliance due to clinical, financial and other situational barriers, creating a plan of care to address patients’ needs. - Assists with the review and revision of departmental policies and procedures, as requested. - Provides managerial responsibilities for the operation of pharmacy in the absence of the pharmacy manager. - Floats from areas of low workload to areas of heavy workload as needed to provide optional patient services Orients and trains new pharmacy personnel, pharmacy interns, students, pharmacy technicians, and flex staff regarding information on scope of practice, policies, and procedures. Work is typically performed in a clinical environment. Accountable for satisfying all job specific obligations and complying with all organization policies and procedures. The specific statements in this profile are not intended to be all-inclusive. They represent typical elements considered necessary to successfully perform the job. Additional competencies and skills outlined in any department-specific orientation will be considered essential to the performance of the job related to that position. Position Details: Education: Bachelor's Degree-Pharmacy (Required) Experience: Minimum of 1 year-Related work experience (Required) Certification(s) and License(s): Licensed Pharmacist (Pennsylvania) within 90 days - State of PennsylvaniaState of Pennsylvania, Licensed Pharmacist - Default Issuing BodyDefault Issuing Body Skills: Teamwork OUR PURPOSE & VALUES: Everything we do is about caring for our patients, our members, our students, our Geisinger family and our communities. - KINDNESS: We strive to treat everyone as we would hope to be treated ourselves. - EXCELLENCE: We treasure colleagues who humbly strive for excellence. - LEARNING: We share our knowledge with the best and brightest to better prepare the caregivers for tomorrow. - INNOVATION: We constantly seek new and better ways to care for our patients, our members, our community, and the nation. - SAFETY: We provide a safe environment for our patients and members and the Geisinger family. We offer healthcare benefits for full time and part time positions from day one, including vision, dental and domestic partners. Perhaps just as important, we encourage an atmosphere of collaboration, cooperation and collegiality. We know that a diverse workforce with unique experiences and backgrounds makes our team stronger. Our patients, members and community come from a wide variety of backgrounds, and it takes a diverse workforce to make better health easier for all. We are proud to be an affirmative action, equal opportunity employer and all qualified applicants will receive consideration for employment regardless to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or status as a protected veteran.

The Company: With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer. Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building. The Role: Reporting to the Head of PV Science, the Associate Director, Drug Safety and Pharmacovigilance Scientist is responsible for assessing and interpreting safety data from multiple sources, including clinical trials, spontaneous and solicited reports, aggregate, and literature reports. This individual is expected to provide interpretation and summaries of drug safety information and provide input in the generation of safety reports (e.g., DSURs, PADERs, PBRERs, and clinical safety assessments). This individual may also support the medical assessment of Individual Case Safety Reports (ICSRs) and other drug safety information. The individual will be an integral part of a group of safety professionals within Nuvalent and will closely collaborate with safety teams in Contract Research Organizations (CROs) and partners. He/she will need to maintain medical knowledge as required by the role, strong and current knowledge of drug safety and pharmacovigilance regulations, pharmacovigilance practices, safety surveillance and risk-management practices. Responsibilities: - Contribute to the generation of aggregate safety reports including development safety update reports, periodic benefit risk evaluation reports, and provide medical input in review of new or existing safety documents to ensure compliance with relevant regulatory requirements, such as protocols, safety summaries and regulatory reports - Contribute to signaling and safety surveillance processes, including the identification of safety observations, emergent safety concerns and new safety signals, ensure prompt assessment and communication of confirmed safety signals - Serve as a medical resource for the generation and review of clinical trial protocols, informed consent forms (ICFs) and investigator brochures (IBs) and the development of Reference Safety Information - Contribute to creation or and updates to Risk Management Plans (RMPs) and/or Risk Evaluation and Mitigation Strategies (REMS) and the maintenance of these documents - Contribute to the development of Standard Operating Procedures, Working Instructions and other guidance documents - Provide safety and pharmacovigilance training programs as required - Collaborate cross functionally (e.g., Reg Affairs, Clin Ops, Clin Science) to ensure pharmacovigilance input - Support the medical assessment of ICSRs as needed - Support other pharmacovigilance and drug safety responsibilities as assigned Competencies Include: - Design global risk management frameworks for Nuvalent’s medicines - Translate safety data into clinical insights - Adapt visualization tools for safety surveillance - Influence multidisciplinary teams to prioritize patient safety. - Strong ability to build relationships, collaborate and influence across disciplines within Nuvalent and with outside stakeholders Qualifications: - 4+ years’ experience in Drug Safety / Pharmacovigilance in a pharmaceutical or biotech company, CRO or regulatory agency - Degree in a medical or healthcare related discipline like MD, PharmD, RN or PhD. - Excellent knowledge of US and EU drug safety regulations, CIOMS and ICH guidelines - Experience with medical drug safety assessments, drug safety surveillance and monitoring activities - Experience with safety data collection and interpretation from clinical trials, literature and post market - Experience with preparation of responses to Regulatory Authorities and experience with IND/NDA submissions and negotiations with Regulatory Authorities as part of marketing approval - Experience with the development and updates to Reference Safety Information, IB, Company Core Data Sheet and local labels - Excellent verbal, written and presentation skills Additional Information: Nuvalent is committed to fair and equitable compensation practices, aiming to provide employees with competitive total rewards packages. The targeted salary range reflects what Nuvalent reasonably and in good faith expects to offer for this position at the time of posting, but the final salary determination may be within or outside this range based on various factors, including, but not limited to, experience, skills, education, and market factors. The range will be reviewed regularly and is subject to change. Nuvalent also offers a comprehensive benefit package to support our employees at each stage of their career, financial, health, and well-being journey, including medical, dental, and vision insurance, 401(k) retirement savings plan, generous paid time off (including a summer and winter company shutdown), and much more. Annual Salary Range $170,000—$195,000 USD Nuvalent provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law. Nuvalent is aware that many companies are dealing with fraudulent job postings on third-party employment search sites and/or individual(s) or entities claiming to be employees of such companies. Those involved are offering fraudulent employment opportunities to applicants, often asking for sensitive personal and financial information, and using such information for criminal activities. Please be advised that all legitimate correspondence from a Nuvalent employee will come from "@nuvalent.com" email accounts. Automated system response emails from our Greenhouse applicant tracking system come from a “no-reply@greenhouse.io” email address. There are no variations of these email addresses and Nuvalent would not request personal and/or financial information via email. Job opportunities would only be extended after a completed job application is submitted by a candidate and a thorough interview process including 1:1 and/or group interviews via phone, video conferencing and/or in-person. If you believe you have been contacted by anyone misrepresenting themselves as an employee of Nuvalent, please contact Nuvalent at 857-357-7000. Thank you.