Please refer to the attached job description and person specification for full details of responsibilities 1. To provide evidence based assessment of participants who were referred to the trial after providing informed consent.2. To formulate and implement treatment plans for psychological treatment in line with the treatment protocol and considering the participants problems. The post holder needs to have the capacity to recognize and identify participants for whom the protocol may not be appropriate. These participants should be allocated to suitable service providers.3. To exercise professional responsibility for the assessment, psychological formulation, treatment and discharge of participants.4. To provide specialist psychological advice, guidance and consultation to other professionals contributing directly to participants formulation, diagnosis and treatment plan within the trial protocol.5. To communicate, in a highly skilled and sensitive manner, to participants and others (e.g., the participants GP) as appropriate, information that may be contentious or highly distressing concerning the assessment, formulation and treatment plans of participants under their care.6. To maintain clinical records and produce clinical reports as appropriate, which adhere to the trial protocol.7. Reliably establish on-going consent throughout a participants trial participation.8. To deal with risk issues.9. To participate in the multidisciplinary systems for monitoring and managing workload as agreed by the professional and line manager.10. To work within levels of professional competence.