Tasneem M. Email & Phone Number

United Kingdom

- Maintaining the investigator site files for commercial funded clinical trials and the trial master site files for Christie sponsored trials.- Develop recruitment and retention plans with the clinical team and ensure they reflect how the study will be facilitated and the potential challenges presented while dealing with patient concerns.- Responsible for ensuring clinical report forms and other data capture mechanisms are completed efficiently and effectively within an agreed… Show more - Maintaining the investigator site files for commercial funded clinical trials and the trial master site files for Christie sponsored trials.- Develop recruitment and retention plans with the clinical team and ensure they reflect how the study will be facilitated and the potential challenges presented while dealing with patient concerns.- Responsible for ensuring clinical report forms and other data capture mechanisms are completed efficiently and effectively within an agreed timeframe, while dealing with closing data queries raised by the data managers.- Ensuring appropriate financial agreements are in place for both commercial and trust-sponsored research- Coordinate site monitoring visits, site initiation visits, and complete recruiting plans to facilitate the efficient start-up of clinical trials for the team. Show less

Manchester, England, United Kingdom

Participated actively in recruitment of participants for COVID-19 clinical trials, gaining valuable experience in overseeing both CTIMP and Non-CTIMP studies. Currently working as part of the collaborative surgery team with a primary focus on setting up and patient recruitment support for HPB and Hepatology portfolios. -Assist in the coordination of clinical research studies, including patient recruitment, informed consent, and protocol adherence.-Collect, record, and maintain… Show more Participated actively in recruitment of participants for COVID-19 clinical trials, gaining valuable experience in overseeing both CTIMP and Non-CTIMP studies. Currently working as part of the collaborative surgery team with a primary focus on setting up and patient recruitment support for HPB and Hepatology portfolios. -Assist in the coordination of clinical research studies, including patient recruitment, informed consent, and protocol adherence.-Collect, record, and maintain accurate and complete research data, adhering to established protocols. Organise and manage research databases, electronic case report forms (eCRFs), and paper records as delegated.-Collaborate with clinical investigators, research coordinators, and other team members to support research objectives.- Maintaining an efficient flow of information with the trust research office, sponsors and outside agencies to ensure the smooth facilitation of studies.-Thorough understanding of the clinical research process, including preparing for research monitoring visits, reviewing regulatory documents, and ensuring all the necessary documents are completed in advance.- Data collection and query completion to the highest standards, resulting in high-quality research in accordance with GDPR regulations.- Developing and implementing study specific recruitment strategies to improve recruitment and ensure study recruitment targets are met.- Monitor patient safety throughout the study, promptly reporting and documenting adverse events or deviations from the protocol. Assist in safety reporting and ensure participants well-being. - Manage the Trial Site Master Files, ensuring documents are meticulously organised and ready for sponsor monitoring visits. - Mentoring new starters and providing ongoing support during their transition period to enable them to thrive in their positions. Show less

Senior Leadership role within the charity organisation. Reporting directly to the UK Director and board of advisors.- Oversee and collaborate with various departments within the UK structure including Events, Finance, institutions and other regional representative leads. - Contribute to the development and review of organisational policies and procedures.- Supervise and mentor department heads and regional represenasative leads by completing frequent 1:1 sessions. - Make… Show more Senior Leadership role within the charity organisation. Reporting directly to the UK Director and board of advisors.- Oversee and collaborate with various departments within the UK structure including Events, Finance, institutions and other regional representative leads. - Contribute to the development and review of organisational policies and procedures.- Supervise and mentor department heads and regional represenasative leads by completing frequent 1:1 sessions. - Make informed decisions to drive the continuous growth and development of the UK team. - Represent the UK team in various international team meetings and being a voice for the team when presenting achievements and lessons learnt. Show less

2020/2019 – National Head of Events 2018 - National Events Team Member - Responsible for overseeing the training and support required for team members. -Developing strategic event plans that align with the organisation goals and objectives for the 6 UK Event teams.- Addressing challenges and issues that may arise within the regions in a prompt and effective manner. - Negotiate with Finance teams to ensure the event budgets are reflective of the needs to each retrospective… Show more 2020/2019 – National Head of Events 2018 - National Events Team Member - Responsible for overseeing the training and support required for team members. -Developing strategic event plans that align with the organisation goals and objectives for the 6 UK Event teams.- Addressing challenges and issues that may arise within the regions in a prompt and effective manner. - Negotiate with Finance teams to ensure the event budgets are reflective of the needs to each retrospective region. - Collaborating with marketing teams to ensure plans are in place for effective marketing campaigns to maximize attendance. 2016/2017 - Midlands Events Team Leader - Develop comprehensive event plans for the Midlands region, including budgets, timelines, and resource allocation, while considering logistics, safety, and regulatory requirements.- Identify and liaise with network of trusted vendors and select suitable venues that align with the events vision and budget as part of the yearly volunteer awards dinner. - Oversee logistics and coordination such as decor, AV system setups, catering and role allocations for a successful event.-Facilitated the planning of mountain treks for group exceeding 200 individuals. Collaborated with Marketing and finance teams to ensure the successful execution of event. -Analyze the event's success by collecting feedback, reviewing objectives, and assessing key performance indicators to refine future event strategies. Show less

-Assist in the coordination of research lead clinics for research patients attending at the Clinical Research Facility (CRF).- Prepare and maintain essential study documentation, including study binders, regulatory documents, and source documents.- Communicate with research participants to schedule appointments.- Complete any clinical activities required to ensure the patient's treatment is completed in a timely manner.

-Tailor care plans to meet the specific requirements and preferences of each client, promoting their physical, emotional, and social well-being.-Conduct in-depth assessments of clients' health, functional abilities, and daily living needs to determine the most effective care strategies.-Maintain ongoing communication with clients and their support networks including GP's, social workers etc to monitor the effectiveness of care plans, making adjustments as necessary to address changing… Show more -Tailor care plans to meet the specific requirements and preferences of each client, promoting their physical, emotional, and social well-being.-Conduct in-depth assessments of clients' health, functional abilities, and daily living needs to determine the most effective care strategies.-Maintain ongoing communication with clients and their support networks including GP's, social workers etc to monitor the effectiveness of care plans, making adjustments as necessary to address changing needs.-Ensure that care plans adhere to regulatory requirements and ethical standards as per CQC requirements while maintaining detailed records of care activities and outcomes.-Acting as an advocate for clients rights, preferences and best interests by facilitating person-centered, high- quality care plans. Show less

Leicester, England, United Kingdom

-Supporting and Guiding Prospective Students-Provide insight and promote academic programs-Organise and participate in university eventsDeliver presentations and speeches at university events, sharing personal experiences and insights.

Education record

Education record