Role Description The College of Nursing and Health Care Professions at GCU is seeking knowledgeable, mission-driven Adjunct Faculty to teach Nursing Research and Evidence Based Practice online. - Deliver engaging, high-quality instruction using innovative teaching methods and current industry technologies. - Maintain compliance with accreditation standards. - Model the holistic tenets of the nursing profession and uphold the University’s mission and pillars. - Facilitate meaningful classroom discussions, assess student learning, and prepare students for leadership roles in health care. - Support program initiatives and demonstrate alignment with the philosophy and direction of the University. - Provide a positive example by supporting GCU’s Doctrinal Statement, Ethical Position Statement, and Mission. Qualifications - A Master's degree (or higher) in Nursing or a Bachelor's in Nursing with a graduate degree in a relevant health care discipline. Graduate degree must be from an accredited university. - Relevant work experience in health care policy, nursing leadership, research, or nursing management preferred. - Must have an active, current, unencumbered RN license with three (3) or more years of direct patient care nursing experience. - Strong communication skills and the ability to build supportive relationships with students. - Proficiency in English, grammar, and APA writing. - Commitment to modeling GCU’s mission and values. Benefits - Tuition benefits specifically for the adjunct employee and dependents. - 401(k). - Employee Perks and Discounts. - Gym and Fitness Center. - Canyon Health & Wellness Center. Required Application Materials Please attach the following when submitting your application: - Unofficial transcripts for all applicable conferred graduate degrees. - Any relevant licenses or certifications.

Role Description The Behavioral Health Research Coordinator is responsible for coordinating and supporting behavioral health studies and clinical trials research across the system. This position works closely with Principal Investigators, the research department, clinical teams, and executive leadership to ensure all studies are conducted in compliance with institutional, federal, and ethical research standards. The Coordinator oversees day-to-day study operations utilizing independent judgment and discretion in: - Participant recruitment - Informed consent - Data collection - Regulatory submissions - Database management - Study documentation This role independently prioritizes competing research activities, recommends process improvements, and collaborates with investigators and leadership on matters impacting study execution, participant safety, compliance, and research outcomes. The ideal candidate is highly organized, detail-oriented, and passionate about advancing evidence-based behavioral healthcare. Consistent with LifeStance’s values, every member of the LifeStance team is expected to support each other and the mission, which may mean participating in projects and initiatives and performing functions and responsibilities not specifically outlined in this job description. Qualifications - Bachelor’s degree in Psychology, Behavioral Health, Social Work, Nursing, Neuroscience, or related field. - Minimum 3 years of experience in clinical and human subjects research. - Knowledge of research methodology, participant confidentiality, and ethical standards. - Strong organizational, communication, and interpersonal skills. - Ability to work effectively with diverse and potentially vulnerable populations. - Proficiency in Microsoft Office Suite and general database management. Requirements - Master’s degree in Psychology, Counseling, Public Health, or related field. - Experience working with behavioral health or addiction populations. - CITI certification, Human Subjects Protection training, or Good Clinical Practice certification. - Qualified candidates must be legally authorized to be employed in the United States. Benefits - Medical, dental, vision, AD&D, short and long-term disability, and life insurance. - 401k retirement savings with employer match. - Paid parental leave. - Paid time off. - Holiday pay. - Employee Assistance Program. Company Description At LifeStance Health, we strive to help individuals, families, and communities with their mental health needs. Everywhere. Every day. It’s a lofty goal; we know. But we make it happen with the best team in mental healthcare. - Belonging: We cultivate a space where everyone can show up as their authentic self. - Empathy: We seek out diverse perspectives and listen to learn without judgment. - Courage: We are all accountable for doing the right thing - even when it's hard - because we know it's worth it. - One Team: We realize our full potential when we work together towards our shared purpose.

Role Description As a CRA at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality outcomes across our clinical programs. This is a sponsor dedicated program focused on monitoring Oncology studies in Montreal. Your role will involve delivering clinical trial monitoring work to a high standard, working closely with your team and stakeholders. - Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation. - Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required. - Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff. - Ensure patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements. Qualifications - University degree in medicine, science, or equivalent. - Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data. - Excellent written and verbal communication in English. - Experience monitoring Oncology studies. - Good social skills enabling you to deal with queries in a timely manner. - Willingness to travel as required (approximately 60%). Requirements - Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Benefits - Competitive base salary and performance related incentives. - Health and wellbeing programmes including medical, dental, and vision coverage where applicable. - Retirement and pension plans. - Life assurance and disability coverage. - Employee assistance programmes and wellbeing resources. - Learning and development opportunities through structured training and career pathways. - Benefits may vary depending on role and location. Company Description ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

Role Description ICF is actively seeking an On-Call Research Analyst to join our growing Workforce Innovations, Preparedness, and Poverty Solutions (WIPPS) team. In this role, you will support research, evaluation, and training and technical assistance projects that promote positive outcomes for vulnerable individuals and families. The Research Analyst will contribute to multiple projects and is ideally based in our Reston, Virginia office. THIS IS AN ON-CALL, part-time hours position based on project needs. - Support the development of written, web-based, and training and technical assistance products, including briefs, reports, tools, and presentations. - Conduct background research and synthesize findings through literature reviews, systematic evidence reviews, evaluation reports, and practitioner- and policy-oriented briefs. - Provide foundational quantitative research and evaluation support, including programming in statistical software and conducting basic statistical analyses. - Assist with qualitative research activities such as instrument development, coding, synthesis, and documentation. - Develop and maintain workflow protocols, templates, and project tracking tools to support high-quality, on-time deliverables. - Contribute to internal knowledge management and support team collaboration across projects. Qualifications - Bachelor’s degree in public policy, sociology, statistics, economics, or a related field. - Minimum 2 years of relevant experience in human services, workforce policy, social policy research, evaluation, or related consulting work. - Demonstrated experience supporting qualitative and/or quantitative research, including exposure to statistical software such as Stata, R, SAS, or SPSS. - Strong technical writing and editing skills. - Proficiency in Microsoft Office applications, including Word, Excel, and PowerPoint. Requirements - Strong organizational skills, attention to detail, and ability to meet tight deadlines. - Analytical and problem-solving skills with sound judgment. - Excellent interpersonal skills and a collaborative, professional approach. - Ability to manage multiple tasks simultaneously in a fast-paced, changing environment. - Strong written and verbal communication skills, including experience supporting presentations. - Self-motivated, proactive, and eager to learn in a team-based setting. Benefits - ICF is a global advisory and technology services provider. - We combine unmatched expertise with cutting-edge technology to help clients solve their most complex challenges, navigate change, and shape the future. - We are an equal opportunity employer. - Reasonable Accommodations are available for disabled veterans, individuals with disabilities, and individuals with sincerely held religious beliefs. - Pay range for this position based on full-time employment is: $61,232.00 - $104,094.00.