• Conduct electronic review of escalated cases against medical policy criteria • Complete initial determination of cases, review of appeals and grievances, and other reviews as assigned • Compose clear and concise rationales for member and provider determination notifications • Participate as a member of the CMDM multidisciplinary team • Advise multidisciplinary team on cases that require physician expertise • Actively manage projects and/or participate on project teams that require a physician subject matter expert

Role Description Fidelia Counseling Services is seeking a dedicated, Board-Certified or Board-Eligible Child and Adolescent Psychiatrist (MD or DO) to join our multidisciplinary clinical team. This role focuses strictly on psychiatric evaluations, medication management, and clinical consultation for children, adolescents, and transitional-age youth. You will work closely with our therapists, CBHI community teams, and the leadership team to provide integrated, high-quality, and trauma-informed psychiatric care to families in our community. Key Responsibilities - Psychiatric Evaluations: Conduct comprehensive diagnostic psychiatric evaluations for children and adolescents presenting with complex emotional, behavioral, and neurodevelopmental challenges (including ADHD, Autism, Bipolar Disorder, and severe trauma). - Medication Management: Safely prescribe, monitor, and manage psychotropic medications for pediatric populations, adhering strictly to pediatric psychopharmacology standards and Massachusetts state monitoring guidelines. - Multidisciplinary Collaboration: Act as the core medical/psychiatric consultant for our clinical team, participating in case consultations and collaborating with therapists, mentors, and the Operations Director to ensure holistic client care. - Documentation & Compliance: Complete psychiatric evaluations, progress notes, and treatment plan sign-offs in our secure Electronic Health Record (EHR) system within standard compliance timelines. Maintain a high standard of HIPAA compliance. - Crisis Consultation: Provide clinical and diagnostic direction during high-risk pediatric psychiatric crises or complex diagnostic presentations. Qualifications - Doctor of Medicine (MD) or Doctor of Osteopathic Medicine (DO) from an accredited medical school. - Successful completion of an accredited General Psychiatry Residency. - Successful completion of an accredited Child and Adolescent Psychiatry Fellowship. - Active, unencumbered medical license in the Commonwealth of Massachusetts. - Board-Certified or Board-Eligible in Child and Adolescent Psychiatry. - Active Massachusetts Controlled Substances Registration (MCSR) and federal DEA registration. - Deep expertise in treating pediatric populations presenting with acute trauma, developmental differences, and behavioral health crises. - Demonstrated commitment to a healthy, non-toxic, and highly collaborative workplace. - Strong alignment with our mission and our motto: "Together we can make it happen." Requirements - Experience working within a community mental health center (CMHC) environment or collaborating with state-funded insurance programs (MassHealth/Carelon/Optum) is a plus. Benefits - Flexible schedule. Position Details - Employment Type: Independent Contractor (1099) or Part-Time (negotiable hours/sessions per week to accommodate private practice splits). - Location: Telehealth (Woburn, MA location with options for integrated telehealth sessions). - Language Competency: Bilingual candidates are highly encouraged to apply. Fluency or clinical proficiency in Spanish, Haitian Creole, or Portuguese is highly preferred to support our diverse patient population, though all qualified prescribers will be considered. - This is a remote position.

• Serve as the lead clinical liaison for partner providers across multiple regions, representing Cadence’s care model with clinical authority and consistency • Partner with PRMs on clinic visits and ongoing relationship management to strengthen long-term program engagement • Communicate the clinical rationale behind Cadence’s care protocols, data practices, and service offerings • Lead onboarding and training for new clinic partners • Resolve provider concerns with empathy, clinical judgment, and structured follow-through to deepen partner relationships • Translate field insights into actionable intelligence for clinical, product, and engineering teams, directly informing service improvements and care model refinement

Title: Medical Director, Clinical Trial Physician - Neurology (Remote) - FSP Location: Remote United States of America Full time Remote Join Thermo Fisher Scientific as a Medical Director/Clinical Trial Physician(FSP) based in the United States and be part of a world-class organization conducting groundbreaking research. Ideal candidate location is Eastern or Central Time Zone. This position is fully remote, benefit eligible with travel in a 10-20% range(international maybe required). *Must be legally authorized to work in the United States or Canada without sponsorship. *Must be able to pass a comprehensive background check, which includes a drug screening(where applicable). *East coast time zone is preferred, or ability to work EST hours Client Dedicated Role: Our client, a global mid-sized biotech company, focuses on developing innovative treatments for patients with autoimmune diseases. This fast-growing, international organization has a strong scientific foundation. If you're looking for a place where your work, in partnership with others, can have real impact—and where you're encouraged to challenge yourself and contribute to breakthrough solutions , the Medical Director/Clinical Trial Physician could be a great fit. Discover Impactful Work: Provides clear medical leadership in the Study team, working in close collaboration with the other members of this cross functional team, in order to provide reliable, high quality study data within time and budget. A day in the Life: - Provide medical leadership to the study teams, including creating clinical trial protocols while implementing the latest scientific information, contribute to site selection, contribute to review and approval of study protocols and amendments, Clinical Study Reports (CSRs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), protocol deviation decisions and other clinical documents as required for the conduct of clinical trials - Real time Medical Monitoring of clinical studies: ensure medical validity of each individual primary endpoint as well study subject safety, while ensuring medical issues are identified early. Pro-active escalation and correction of issues in consultation with the Global Medical Indication Lead - Interpret the clinical trial data for regulatory documents (e.g. CSR, INDs, Annual Reports, NDAs, MAAs, etc.), manuscripts, and other publications as required, in consultation with the Indication Lead - Medical point of contact for all internal and external stakeholders: Interact with the investigators as needed, answer questions of IRBs and Health Authorities, prepare and present material to the study executive and independent safety committee if applicable; medical training of site staff at Investigator meetings; CRA training in new indications - Ensure study compliance for all medical aspects by understanding and applying all relevant SOPs and GCP - Closely collaborate with the cross functional study team members in order for medical risks, issues, and results to be clear to all involved parties - In case more than 1 physician is working on the protocol, a primus inter pares will be appointed, and they will ensure that answers to questions from sites /IRBs RAs, eligibility and protocol deviation decisions will be harmonized across medics Keys to Success: Education - Medical Doctor or equivalent degree required. Board certification(s) are preferred - Specialty education(e.g. residency/fellowship) required in neurology. This should be accompanied by patient treatment and/or research experience - 1-3 years of industry experience required. Experience should be in clinical development in a Pharmaceutical, Biotech or CRO organization - Neurologists with expertise in Pediatric Neurology or Neuromuscular diseases are highly preferred. Knowledge, Skills, Abilities - Excellent English, both written and spoken is a must, as well as ability to travel - Shown understanding and experience with NDA submission process - Shown understanding of regulatory guidelines for adverse event reporting - Proven interpersonal skills enabling to lead a study team, while recognizing individual expert competencies, providing medical advice and evaluations exercising judgment in which issues need to be escalated immediately - Pro-active problem solver with negotiation skills, remaining sensitive to the different cultural needs in a global organization - Strong communication skills to ensure close collaboration with the cross functional team members so that study plans and status are transparent, and that risks, issues, and results are clear to all involved parties. A matrix structure requires additional skills in gathering decision information, negotiation and communicating decisions and actions Benefits We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!