• Conduct comprehensive assessments of behavioral, emotional, and mental health needs • Develop individualized treatment plans aligned with client goals • Provide evidence-based individual, family, and group therapy using modalities such as CBT and DBT • Deliver care both onsite and virtually in alignment with the hybrid care model • Track client progress and adjust treatment plans as needed • Maintain accurate and timely clinical documentation, including progress notes and treatment outcomes • Work collaboratively with Primary care physicians, psychiatrists, social workers, case managers, and other healthcare professionals • Provide crisis intervention and support to clients in acute distress • Educate clients and families on mental health conditions, treatment options, and coping strategies

Role Description At Spring Health, we’re on a mission to revolutionize mental healthcare by removing every barrier that prevents people from getting the help they need, when they need it. The Specialty Care Navigator – Eating Disorders will provide assessment, care coordination, and clinical support for members navigating eating disorder care. This remote role is part of the Care Navigation team and plays a critical role in delivering high-touch clinical support within our innovative specialty care vertical. The required schedule for this opportunity is Monday to Friday from 9am-5pm PDT or MDT. What You’ll Be Doing - Conduct telephonic screenings, brief interventions, and refer members to appropriate eating disorder treatment - Apply active listening, psychoeducation, and motivational interviewing to support member goals - Coordinate care plans and facilitate referrals within the Spring Health network - Provide crisis management and safety planning as needed - Maintain accurate and timely documentation within internal systems and EHR - Collaborate with cross-functional teams (care support, provider ops, billing, etc.) - Contribute to program development, team onboarding, and process improvements What Success Looks Like - Timely connection of members to appropriate care - High care conversion rate and positive clinical outcomes - Strong member satisfaction (CSAT) and engagement - Consistent documentation and follow-up within required timeframes - Effective collaboration across teams Qualifications - Independently licensed mental health professional (LCSW, LMFT, LPC) - firmly required - Ability to work Monday through Friday, 9am-5pm PDT or MDT - firmly required - 2+ years of clinical experience working with eating disorders - firmly required - Proficiency with motivational interviewing, diagnostic assessment, and triage - Knowledge of evidence-based treatments for ED (CBT-E, Family-Based Treatment) - Strong communication, organizational, and tech skills - Commitment to diversity and inclusion - Bilingual proficiency - preferred - Experience in working with adolescents - preferred Requirements - The target base salary range for this position is $33.33 - $42.31 hourly - Part of a competitive total rewards package including stock options and benefits - Individual pay may vary from the target range and is determined by a number of factors including experience, location, internal pay equity, and other relevant business considerations Benefits - Health, Dental, Vision benefits start on your first day at Spring - Access to One Medical accounts - HSA and FSA plans available, with Spring contributing up to $1K for HSAs, depending on your plan type - Employer sponsored 401(k) match of up to 2% for retirement planning - A yearly allotment of no cost visits to the Spring Health network of therapists, coaches, and medication management providers for you and your dependents - Competitive paid time off policies including vacation, sick leave, and company holidays - Parental leave of 18 weeks for birthing parents and 16 weeks for non-birthing parents after 6 months tenure - Access to Noom, a weight management program tailored to your unique needs and goals - Access to fertility care support through Carrot, with $4,000 reimbursement for related fertility expenses - Access to Wellhub, connecting employees to fitness, mindfulness, nutrition, and sleep options - Access to BrightHorizons, providing sponsored child care, back-up care, and elder care - Up to $1,000 Professional Development Reimbursement a year - $200 per year donation matching to support your favorite causes

Role Description The Specialty Access Center (SAC) is an inbound, fast-paced, high-volume center with an average of 6,000 calls per day. The SAC supports multiple Adult and Pediatric Specialties, which include: - Cardiology - Dermatology - ENT - Med-Surg - Neuroscience - Oncology - Ophthalmology - Primary Care - Pulmonology - Solid Organ Transplant - Urology - Women’s Health As the first point of contact, the SAC provides essential support in connecting patients with the care they need. What you will do as a Patient Access Scheduler: - Uses technology proficiently to identify and satisfy patient appointment scheduling needs. - Coordinates all aspects of patient scheduling needs according to protocols. - Notifies caller of change in appointment scheduling. - Acquires patient demographic and insurance information for new patients and verifies for returning patients. - Can optimally determine when a conversation needs to be escalated to triage or manager. - Provides pre-appointment instructions to patients at the time of the call. - Responds to, answers and/or advises questions or concerns. Qualifications - HS Diploma/GED - 1+ Years Customer Service experience in healthcare or professional service industry - Proven ability to listen effectively, maintain HIPAA-compliant confidentiality, and resolve patient complaints while demonstrating patience and professionalism - Strong telephone management, organization, and prioritization skills Requirements - This position requires a full month of uninterrupted training. - Location: At this time, this position will be working remote (MN residents only). - Hours: Monday - Friday, 8:30am-5:00pm. Benefits - Generous benefit package including but not limited to: - Medical, dental, vision plans - Life insurance - Short-term and long-term disability insurance - PTO and Sick and Safe Time - Tuition reimbursement - Retirement - Early access to earned wages - And more! - Please follow this link for additional information: Fairview Benefits Company Description EEO/Vet/Disabled: All qualified applicants will receive consideration without regard to any lawfully protected status.

Title: Patient Safety Associate I - Drug Safety Associate I Location: United States-North Carolina-Remote Job Description: When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Make a Meaningful Impact in Global Patient Safety At Parexel, we’re dedicated to improving patient health worldwide. As a Patient Safety Associate I, you’ll play a vital role in supporting drug safety, clinical trials, and post‑marketing surveillance activities in post-market surveillance, with some exposure to clinical trials, ensuring full compliance with regulatory requirements and Standard Operating Procedures (SOPs). As a Patient Safety Associate I, you'll be responsible for several key activities including processing Individual Case Safety Reports (ICSRs) from multiple sources with accuracy and efficiency, conducting comprehensive literature searches and reviews to identify safety signals, and supporting signal detection and management activities. You'll track and monitor regulatory information updates, assist in preparing and executing regulatory submissions, and contribute to the development of aggregate reports and study-specific safety documents. Where applicable, you'll also manage Medical and Product Dictionary activities. Your role will be crucial in maintaining compliance through quality reviews of safety deliverables, generating metrics and performance indicators for safety operations, investigating and documenting late deliverable incidents, and ensuring adherence to international and local regulatory reporting requirements. We're looking for candidates with strong attention to detail and commitment to quality, an understanding of drug safety regulations and pharmacovigilance principles, excellent organizational and time management skills, the ability to work collaboratively in a team environment, and strong written and verbal communication skills. Join a global leader in Clinical Research Organization services, where you'll contribute to improving patient safety worldwide while developing your career in pharmacovigilance. What You’ll Do: General Safety Operations - Follow project-specific procedures and regulatory standards. - Support basic compliance activities, documentation, metrics, and audit preparation. - Work collaboratively with team members and complete required training programs. ICSR (Individual Case Safety Report) Processing - Review, triage, and process safety reports from various sources. - Perform data entry in safety databases with accuracy and medical consistency. - Assist with follow-ups, case narrative preparation, MedDRA coding, and quality checks. - Support compliance investigations and metrics reporting. - Prepares medically cohesive case narratives based upon the reported information. Safety Submissions - Submit ICSRs and periodic safety reports to Health Authorities and stakeholders. - Maintain regulatory submission schedules and reporting rules. - Assist in audit preparation and regulatory intelligence updates. - Support global reporting configuration and compliance activities. Literature Search & Review - Develop and maintain literature search strategies. - Screen published articles for potential safety signals or adverse events. - Conduct quality checks and manage journal reviews. - Collaborate with internal teams for full-text retrieval and assessment. Affiliate Services - Support communication between global operations and local safety affiliates. - Assist with safety information exchange, translations, and compliance tasks. - Conduct literature monitoring and data reconciliation activities. Regulatory Support - Maintain regulatory systems and product registrations. - Assist with submissions (eCTD), renewals, variations, and lifecycle management. - Verify data accuracy and generate quality and compliance reports. Regulatory Intelligence - Research and maintain global safety reporting requirements. - Update regulatory intelligence databases and trackers. - Support day-to-day operations within the Global Pharmacovigilance Intelligence Office. Your Knowledge & Experience: - Foundational knowledge of drug safety regulations and pharmacovigilance processes. Ideal candidate has 3+ years experience in Drug Safety. - 2+ years experience in a post marketing. - Experience in multiple therapeutic areas (cardiology, neurology, oncology, rare disease). - Strong attention to detail, organizational skills, and problem‑solving ability. - Effective communication and willingness to work in a collaborative team environment. - Proficiency with MS Office and ability to learn safety systems/databases. Preference for those with Veeva Safety experience. Education - Bachelor’s degree in Life Sciences, Health Sciences, Biomedical Sciences (e.g., Pharmacy, Microbiology, Biochemistry, Biotechnology) or equivalent education/experience. This role offers the flexibility to work from home in the US. #LI-KS1 EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.