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PowerPoint Presentation Module 8 Managing Communication and Managing Risks Building rapport Building healthy collaborative working relationships is vital on a study team. You with each person,...

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PowerPoint Presentation
Module 8
Managing Communication and
Managing Risks
Building rapport
Building healthy collaborative working relationships is vital on a study team. You with each person, and between other team members.
Important to establish connections based on different personalities, interests, working styles, etc. Take an interest in what is of interest to others.
Building rapport
Be a reliable team member – follow through and do what you say you will do. Apologize when needed.
Keep confidences when asked (and if you can't, say so)
Demonstrate respect for all team members in your conversations. Save any concerns you might have about individual performance for discussions with the person themselves.
Communication
Open and two-way
Say specifically what is needed and/or...
Ask for input and ideas on tasks and projects
Discuss what is needed and who will do
Repeat back the feedback/decision
Communication
Ask what the person needs in order to accomplish
Decide timelines (by when) - Urgent? Less so?
Check for understanding
When communication isn't enough/adequate, find other ways, state the issue and problem solve with the person, etc.
Explore various tools – text, email, team huddles, 1:1s, etc
Planning and communication meetings might include
Internal
Programmatic/divisional priority meetings
Nuts and bolts planning and implementation meetings with study team
PI huddles
Budgets/contracts meetings
Other groups as needed
External
Sponsors
Multisite collaborations
Local subs
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Communication plan example
Risk management
Anticipating, planning, and responding to risks
Risk in research
Research is inherently risky because it is often investigating the unknown
Some amount of risk is necessary in order to fuel innovation
But, there are project-related risks which can derail progress which need to be proactively identified and managed
Common risks in clinical research
Technology issues
Inefficient processes
Supply delays
Institutional ba
iers
Recruitment problems
Forecasting risks
Take a look at the protocol with your team (the more experience and eyes, the better)
Can you identify tasks or processes that might be challenging to accomplish?
Are there parts of the protocol that are contingent on each other?
Are there supplies or equipment needed?
Are there other internal or external groups that execute part of the protocol (like a lab or clinical team)?
What institutional or other processes might be needed (besides IRB, will you need IBC, administrative approval, etc.)?
Are there other institutions involved and what do they require?
Risk planning
As much as possible, plan out what your team will do to try to mitigate the known risks (timelines, prioritization, etc.)
Write a plan for each risk – look at potential problems and plan for them
Example – risk of outside lab needed for research. What steps will you need to take to find out what paperwork or processes or funding etc. is needed to involve this lab? Will contracts be needed and if so what are the process risks with those?
Example – multiple committee approvals needed. What order do they need to be done in? What are some of the known issues/delays with each group?
Think about the unknown risks and how you might identify, escalate, and address those as they come up
Manage the unexpected
Successful projects have proactive leaders and teams
Have an SOP in place for risk and issue management
Very important to develop risk assessment with entire team/collaborators in order to get multiple perspectives
Risks should be reviewed by the study team on a regular basis
Blanco, H. June 18, 2020. Dealing with the unexpected: Covid-19 and risk management. Clinical Trials. https:
www.clinicaltrialsarena.com/analysis/clinical-trial-risk-management/​
Cornerstones of risk management
Strategize (successful study implementation)
Problem solve potential pitfalls (of study implementation)
Anticipate problems (with study population, vendors, resources, funding, staffing, sites, and others)
Have systems in place to deal with issues when they arise
set up redundancies of effort/cross training when possible
make sure issues are regularly discussed and escalated
team should identify the abnormal whenever it comes up
discuss risks whenever talking about projects and tasks
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SOP for risk management
How frequently risk will be assessed
Cross functional team involvement in risk assessment
Risk score based on impact and likelihood
Proactive actions to reduce risk
Pre-defined actions to take if risk becomes an issue
Blanco, H. June 18, 2020. Dealing with the unexpected: Covid-19 and risk management. Clinical Trials. https:
www.clinicaltrialsarena.com/analysis/clinical-trial-risk-management/
Answered 1 days After Nov 04, 2022

Solution

Dr Insiyah R. answered on Nov 05 2022
48 Votes
Introduction    2
Conclusion    4
Reference    5
Introduction
Effective patient recruitment for research often includes locating eligible populations, recruiting a sufficient and/or representative sample, keeping participants involved until the study is done, and keeping costs low without sacrificing the quality of care or ethics (Clark et al,2019). Methods that improve patient recruitment for primary care studies are this piece's topic. Strategies that include clinicians and/or their practices and the patient directly fall under this category. This assignment aims to draw attention to the need for effective recruiting and retention strategies for research participants, especially in the setting. The most prevalent recruiting practices and the variables that impact them will also be covered.
Finding people to participate in primary care research studies might take a long time because of the difficulty of recruiting patients. It's because of institutional, expert, and individual challenges. Inadequate allocation of resources, governance systems that stymie decision-making, inefficient communication routes, and administrative challenges all contribute to the difficulties faced by an organisation (Inan et al,2020). Several obstacles, both on the side of professionals and patients, were uncovered in a systematic study of people's willingness to take part in randomised controlled trials. According to the authors:
Time constraints, a lack of staff and training, concern about the impact on the doctor-patient relationship; patient concerns, loss of professional autonomy; difficulty with the consent procedure; a lack of rewards and recognition; and an inadequately interesting question were all cited as obstacles faced by clinicians. Additional trial requirements, patient preferences, anxiety over the unknown, and informational and consent-related fears posed difficulties for trial participants (Julian McFarlane et al,2022).
It may be pricey to recruit patients inefficiently. Costs may be
oken down into three categories: monetary, intellectual, and individual. Money is spent on things like research materials and employee time on extending projects so that new and creative recruiting methods may be found and implemented. Lost chances for therapeutic innovation and stalled publishing schedules are two examples of the knowledge costs that slow the spread of new discoveries. Adverse individual outcomes, such as the extension of illness and the stress on caregivers, might result from patients having to wait longer for access to novel medicines since the results may not be generalizable and valid.
A representative sample shouldn't be exclusively...
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