Salima Aamdani

- Ensure accurate conduct of all aspects of clinical trials according to trial protocols including, liaising with all internal and external stakeholders and the Ethics Committee.

- Preparation of reports, submissions, advice of amendments and safety notifications, and participate in all audits as required by regulatory authorities.

- Attend conferences and meetings relating to clinical trials research as required, nationally and internationally.

- Responsible for all activity relating to the Study Protocol undertaking, including taking active steps to read and maintain a working knowledge of the protocols, organising diagnostic investigations and interventions as per protocols.

- Undertaking all aspects of patient recruitment including explanation of trials, informed consent, follow up and other needs as required.

- Have a demonstrated knowledge of a range of research approaches and their application within clinical trials.

- Ability to collect, analyse and evaluate information effectively, to contribute to decisions and recommendations in a consultative environment.

• Coordinate the implementation and evaluation of TeleClinical Care Remote Monitoring project.
• Managing Investigator-led/Commercially Sponsored clinical trials, research projects and registries.
• Screening and recruiting patients for clinical trials and monitoring and recording clinical data in REDCap and Medidata Rave.
• Coordinating HREC and RGO ethics applications and managing research agreements CTRA.
• Managing CTMS and databases, including data cleaning, data management and quantitative/qualitative data analyses.
• Preparing grant applications, budgets, technical reports, protocols and manuscripts for publication.
• Maintaining strong relationship with internal and external stakeholder’s including government agencies, academic institutions, and hospital stakeholders.
• Coaching and mentoring team members and contributing to develop work manual for staff education.

• Planned, developed, implemented and evaluated clinical research projects.
• Assisted in the care coordination of patients undergoing in the trials and managing project specific resources.
• Ensured the treatment and data collection is in accordance with the Good Clinical Practice guidelines.
• Timely reporting of adverse events and monitoring care throughout the trial duration.
• Coordinated data management, data analysis and report writing.

• Lead planning and execution of non-communicable disease research projects.
• Created and managed project plans, budgets, and timelines.
• Mentored the team of researchers and support staff members.
• Disseminated research information and promote the implementation of research findings into better patient management.
• Prepared ethics applications, grant applications, abstracts and manuscripts for publication and presented the research progress to investigators and administrators.

• Developed evidence-based Clinical Practice GRADE guidelines using GRADEPRO software in collaboration with The U.S. GRADE Network.
• Contributed in developing Manual of Therapeutics covering the clinical guidelines to manage diseases.
• Conducted research and systematic reviews on disease process.
• Coordinated the translation of research into clinical practice intended to optimize patient care.
• Collaborated with clinical investigators, clinical experts and hospital administrators to formulate clinical practice guidelines.
• Prepared manuscripts for publication and presented the research findings to stakeholders and administrators.

• Facilitated quality improvement and patient safety internal and external audits of clinical specialties.
• Coordinated clinical quality rounds and audited clinical skills and documentation and conducted in service session on clinical best practice standards.
• Managed patient feedbacks, data analysis and report writing/trends on patient experience.
• Managed complaints and incident reporting and coordinated with line managers to ensure patient satisfaction and wellbeing.
• Facilitated the hospital Anesthesia and Surgical Care committee in developing policies and SOPs.
• Prepared periodic reports which includes audit findings, key performance indicators and suggestions to improve overall patient care in the hospital.
• Assisted clinical specialties during accreditation and facilitated visits/inspections of regulatory bodies.

• Conducted initial assessment and head-to-toe assessment of all the patients under her care.
• Collaborated with multidisciplinary teams in planning patient care and assessed patients’/families’ health education needs and intervene accordingly.
• Administered medications and monitored patient responses to medications and report any related incidents.
• Assisted in handling cardiac arrest situations.
• Provided nursing care according to patients' needs in compliance as well as documented patient progress, events, consent forms and patient charting according to hospital protocols.
• Followed admission, transfer, hands off (bedside over) and discharge process according to hospital protocols.

• Conducted head-to-toe assessment and assessed health education needs and intervened accordingly.
• Collaborated with interdisciplinary teams to plan and implement patient care.
• Administered medications, procedures and treatments and managed discharge processes.
• Provided and documented nursing care according to patient needs as per protocols and standards.