Role Description Como Psicólogo/a Clínico/a na knok, terás a missão de prestar cuidados de saúde mental através de vídeo consultas, garantindo um acompanhamento próximo, humano e baseado na evidência. Irás realizar avaliações psicológicas, estabelecer diagnósticos e desenvolver planos de tratamento individualizados, ajustados às necessidades de cada paciente. - Vídeo consultas, avaliações psicológicas e diagnósticos de saúde mental; - Desenvolver e implementar planos de tratamento para pacientes com problemas de saúde mental; - Fornecer terapia individual, familiar e de grupo; - Trabalhar em colaboração com outros profissionais de saúde para fornecer cuidados abrangentes aos pacientes; - Manter registos e relatórios precisos e atualizados de todas as atividades de atendimento. Qualifications - Mestrado em Psicologia Clínica; - Registo profissional válido na Ordem dos Psicólogos; - Experiência em atendimento clínico a crianças e jovens (obrigatório); - Mínimo de 3 anos de experiência na área; - Fluência em inglês; - Conhecimento das técnicas de terapia e intervenções psicológicas; - Habilidade em trabalhar em equipa e em colaboração com outros profissionais de saúde; - Fortes habilidades de comunicação e relacionamento interpessoal; - Disponibilidade para trabalhar em horário pós-laboral e fins de semana; - Autonomia Clínica. Requirements - Experiência com plataformas de Saúde Digital; - Disponibilidade imediata.

Title: Clinical Documentation Integrity Coordinator Location: Florida United States Job Description: Join the team that is revolutionizing health care – BayCare Health System Our network consists of 16 community-based hospitals, a long-term acute care facility, home health services, outpatient centers and thousands of physicians. With the support of more than 30,000 team members, we promote a forward-thinking philosophy that’s built on a foundation of trust, dignity, respect, responsibility, and clinical excellence. Title: Clinical Documentation Integrity Coordinator Facility: Remote (Must Reside in the State of Florida) Responsibilities: - Seasoned CDI professional, proficient in the delivery of the Clinical Documentation processes, with a strong understanding of DRG documentation requirements and coding guidelines, and demonstrating effective leadership skills. - Responsible for designing, conducting, and facilitating educational efforts and trainings related to clinical documentation, as well as sharing ongoing coding guidelines, rules and regulations updates. - Responsibilities include developing, maintaining, and conducting orientation of new CDI team members and Physician Advisors. - Assisting with the assessment, development, and growth of CDI specialists, and acting as a mentor and role model in the profession. - Perform secondary chart reviews and audits for quality assessment of the work provided by the CDI Specialists, and partners with the CDI Supervisors and Manager to create tailored individual education plans. - Assist with the day-to-day coordination of the CDI program including monitoring/balancing/assigning workload, running and reviewing CDI reports to ensure proper reconciliation and management of records through the software application, and performing other duties as assigned. - Must have knowledge of coding guidelines, rules, and regulations - Requires travel between assigned facilities and strong organizational and self-governance skills. BayCare offers a competitive total reward package including: - Benefits (Medical, Dental, Vision) - Paid Time Off - Tuition Assistance - 401K Match and additional yearly contribution - Annual performance appraisals and team award bonus - Family resources and wellness opportunities - Community perks and discounts Experience: - Required - 5 years RN experience in Acute Care - Required - 2 years working as a Clinical Documentation Integrity Specialist Certification - Required - RN - Florida Department of Health - Required - CCDS - Association of Clinical Documentation Integrity Specialist - Preferred - CCS - American Health Information Management Association - Preferred - CDIP - American Health Information Management Association Education - Required - Associates - Nursing - Preferred - Bachelors - Nursing Status: Full Time, Exempt: Yes Shift Hours: 8:00am - 4:30pm (Flexible) Equal Opportunity Employer Veterans/Disabled

• responsible for the successful execution, enrollment and quality of clinical trial portfolio • develop operational strategies and quality plans for all programs and studies • collaborate with other TA directors, local and regional stakeholders • ensure oversight and line management of Clinical Research Manager (CRM) team • lead a team to high performance and accountable for CRM performance reviews.

Title: Medical Device & Diagnostics - CRA 2 - US Remote Location: United States Job Description: Remote United States Remote Illinois Remote California Remote Florida Remote New York View All 15 Locations time type Full time job requisition id 262114 We are currently seeking Experienced Device CRA 2s to lead and support our Medical Device & Diagnostics team! Open to major hub locations across the US. 60-70% travel, 7-9 DOS per month. WHAT YOU WILL DO You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situations based upon clinical research standards. Responsibilities: - Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned - - Responsible for all aspects of site management as prescribed in the project plans - General On-Site Monitoring - Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study - Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements - Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data - Responsible for all aspects of registry management as prescribed in the project plans - Undertake feasibility work when requested - Complete Serious Adverse Event (SAE) reporting, process production of repo11s, narratives and follow up of SAEs - Independently perform CRF review; query generation and resolution against established data review guidelines on Fortrea or client data management systems as assigned by management - Assist with training of new employees, eg. co-monitoring - Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable) and may act as a local client contact as assigned - Perform other duties as assigned by management Requirements - University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure) - 1-3 years of Clinical Monitoring experience - Open to various hub locations The important thing for us is you are comfortable working in an environment that is: - Fast paced: where no deviations from the study protocol are allowed, and not meeting a timeline for even few minutes will create a quality issue. - Changing priorities constantly asking you to prioritize and adapt on the spot. - Teamwork and people skills are essential for the study to run smoothly. - Technology based. We collect our data directly into an electronic environment. What do you get? Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including but not limited to: - Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers) - 401(K) - Paid time off (PTO) – Flex Plan - Employee recognition awards - Multiple ERG’s (employee resource groups) - Target Pay Range (based on title): $105-117K Work Environment: - Work is performed in an office environment with exposure to electrical office equipment. - Frequent travel to clients/ site locations with occasional travel both domestic and international. Physical Requirements: - Ability to sit for extended periods and operate a vehicle safely. - Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists. - Occasional crouching, stooping, with frequent bending and twisting of upper body and neck. - Ability to access and use a variety of computer software developed both in-house and off-the-shelf. - Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs. - Regular and consistent attendance. - Varied hours may be required. #LI - Remote