Staff - Non Union Job Category M&P - AAPS Job Profile AAPS Hourly - Counsellors/Psychologists, Level C Job Title Clinical Psychologist- HOLD Trial Department Bouchard Laboratory | Department of Obstetrics and Gynaecology | Faculty of Medicine Compensation Range $54.64 - $85.21 CAD HourlyThe Compensation Range is the span between the minimum and maximum base salary for a position. The midpoint of the range is approximately halfway between the minimum and the maximum and represents an employee that possesses full job knowledge, qualifications and experience for the position. In the normal course, employees will be hired, transferred or promoted between the minimum and midpoint of the salary range for a job. Posting End Date June 20, 2026 Note: Applications will be accepted until 11:59 PM on the Posting End Date. Job End Date June 30, 2027 This is an hourly position for up to 10 hours per week . At UBC, we believe that attracting and sustaining a diverse workforce is key to the successful pursuit of excellence in research, innovation, and learning for all faculty, staff and students. Our commitment to employment equity helps achieve inclusion and fairness, brings rich diversity to UBC as a workplace, and creates the necessary conditions for a rewarding career. Job Summary Provides cognitive-behavioural couple therapy (CBCT) for individuals with sexual interest/arousal disorder and their partners as part of the Helping with Outcomes for Low Desire randomized clinical trial (HOLD Trial). The trial therapist will follow a 16-session manualized intervention to provide CBCT for couples coping sexual interest/arousal disorder (SIAD). Each session is conducted online and video recorded, via UBC Zoom, over 18 weeks. The trial therapist will carry a caseload of up to 5 couples/week, depending on pace of enrollment in the HOLD Trial. Organizational Status The Psychology, Health, and Sexuality (Phase) Lab in the UBC Department of Obstetrics and Gynaecology (PI: Dr. Katrina Bouchard, RPsych) aims to improve the assessment and treatment of sexual concerns for women, gender diverse people with vulvas, and their partners. The trial therapist will work under the direction and supervision of Dr. Bouchard and with the Research Coordinator(s) for the HOLD Trial. The 3-site HOLD Trial (NCT06777277) is funded by the Canadian Institutes of Health Research. Work Performed · Conducts psychological assessment and provides CBCT services to individuals with sexual interest/arousal disorder and their partners · Engages in case management and contributes to documentation by preparing concise session summaries in collaboration with the PI · May supervise PhD practicum students for diagnostic assessments of SIAD Consequence of Error/Judgement The trial therapist will exercise professional judgment in CBCT sessions. Consequences of inappropriate judgment could include inadequate or inappropriate clinical care and professional liability Supervision Received The trial therapist will complete a structured training program for couple-based sex therapy and CBCT under the supervision of Dr. Bouchard before starting with cases. They will prepare brief session notes and participate in weekly clinical supervision from Dr. Bouchard, including case discussion and review of session video recordings. All trial therapists will participate in weekly clinical supervision, regardless of registration status or level of experience, to align with research protocols for the HOLD Trial. Supervision Given Opportunity to supervise PhD practicum students for diagnostic assessments of SIAD. Minimum Qualifications Ph.D. in Counselling Psychology or a related field. Eligible for certification as a Registered Psychologist in British Columbia. Minimum of seven years of experience in clinical counselling plus experience supervising Doctoral level practicum students. - Willingness to respect diverse perspectives, including perspectives in conflict with one’s own - Demonstrates a commitment to enhancing one’s own awareness, knowledge, and skills related to equity, diversity, and inclusion Preferred Qualifications - Clinical experience providing cognitive-behavioural therapy and sex therapy or have coursework in human sexuality or related topics and/or sex research training is preferred. - Awareness and application of relevant laws, ethical guidelines, and the College’s Code of Conduct relevant to the practice of psychology. - Commitment to the scientific basis of clinical psychology and the integrity of research protocol for the HOLD Trial, including adherence to the manualized CBCT intervention. - Couple therapy graduate coursework and/or clinical experience. - Ability to work independently and as part of a team with excellent communication skills (written and verbal). Ability to problem solve and use flexible judgment in unfamiliar situations. Excellent organizational skills and attention to details.

Clinical Site Associate ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development Clinical Site Associate (CSA) Open to candidates located anywhere in the USA. ICON is currently seeking a Clinical Site Associate (CSA) to join our diverse and dynamic team. We are looking for candidates with a minimum of one year of experience as a Study Coordinator in clinical research. In this role, you will play a pivotal part in supporting clinical trial operations by ensuring site compliance, maintaining accurate documentation, and supporting audit and inspection readiness. The position involves close collaboration with Clinical Research Associates and cross-functional teams to ensure efficient and high-quality trial execution. . What you will be doing Site Support & Oversight: - Manage site-level communications - Coordinate site trainings and systems access - Support site readiness activities including pre/post site visit tasks - Follow-up on action items Document Management: - Maintain Trial Master File (TMF) Your profile - Candidates must have completed a Bachelor’s degree in a relevant field, such as Life Sciences or Healthcare. - Previous experience in clinical research or a related field preferred - Strong organizational and communication skills - Ability to work independently and collaboratively in a fast-paced environment - Attention to detail and ability to prioritize tasks effectively What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: - Various annual leave entitlements - A range of health insurance offerings to suit you and your family’s needs. - Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. - Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being. - Life assurance - Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here. Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

Benefits/Perks - Career Advancement Opportunities - Great Work Environment - Competitive Compensation Job Summary We are seeking an experienced Clinical Supervisor to join our team! As a Clinical Supervisor, you will oversee a team of practitioners and assist with their patient caseload and treatment plans, as well as oversee your own patients. In addition, you will be responsible for meeting with staff, addressing concerns, and helping conduct training and development of existing and new staff members. The ideal candidate has a strong understanding of Applied Behavior Analysis, managing caseloads, and strong interpersonal skills to manage a team. Responsibilities - Conduct regular meetings with staff and advisory boards - Oversee training and development of new and existing staff - Ensure compliance with state and federal regulations - Provide strong leadership and guidance to staff in regards to scheduling and treatment plans Qualifications - Previous experience as a Clinical Supervisor is desired - The required licensing/certification to perform this role - Excellent written and verbal communication skills - Deep understanding of health care policies and regulations - Demonstratable ability to manage others, including handling scheduling and problem-solving Flexible work from home options available.

• Participate in the development, conduct and reporting of corporate/global clinical trials • Understand and keep updated with the pre-clinical and clinical data relevant to the product(s) • Collaborate with the appropriate leaders in the development and maintenance of clinical strategy • Plan, collaborate on, and review the scientific content of clinical documents such as protocols, informed consent documents, final study reports, and submissions • Monitor patient safety during the conduct of studies and conduct the appropriate tracking and follow-up of adverse events • Participate in development and review of label changes and labeling modifications