It is useful to remember that even administering a research questionnaire can have adverse effects on individuals. Problems Anticipated This section should discuss the difficulties that the investigators anticipate in successfully completing their projects within the time frame stipulated and the funding requested.
Project Management This section should describe the role and responsibility of each member of the team Ethics The protocol should have a description of ethical considerations relating to writing research protocols template for resume study. Name and title of the investigator s who is are responsible for conducting the research, and the address and telephone number s of the research site sincluding responsibilities of each.
This should include the timing of assessments. It should stand on its own, and not refer the reader to points in the project description. If multiple sites are engaged in a specified protocol, methodology should be standardized and clearly defined.
Safety aspects of the research should always be kept in mind and information provided in the protocol on how the safety of research participants will be ensured. Duration of the Project The protocol should specify the time that each phase of the project is likely to take, along with a detailed month by month timeline for each activity to be undertaken.
If experimental, it may be described as a controlled or a non controlled study. The statistical methods proposed to be used for the analysis of data should be clearly outlined, including reasons for the sample size selected, power of the study, level of significance to be used, procedures for accounting for any missing or spurious data etc.
This ensures that each group of participants will get the information they need to make an informed decision. For the same reason, each new intervention also requires a separate informed consent form. For guidance on how to write an informed consent form, click here.
They create a setting for the proposal. Study goals and objectives Goals are broad statements of what the proposal hopes to accomplish. General information Protocol title, protocol identifying number if anyand date. Quality Assurance The protocol should describe the quality control and quality assurance system for the conduct of the study, including GCP, follow up by clinical monitors, DSMB, data management etc.
The design of the study should include information on the type of study, the research population or the sampling frame, and who can take part e. This can include procedures for recording and reporting adverse events and their follow-up, for example.
Objectives should be simple not complexspecific not vagueand stated in advance not after the research is done. Recommended format for a Research Protocol Part 1 Project summary Like the abstract of a research paper, the project summary, should be no more than words and at the most a page long font size 12, single spacing.
For projects involving qualitative approaches, specify in sufficient detail how the data will be analysed. It should also offer possible solutions to deal with these difficulties. Expected Outcomes of the Study The protocol should indicate how the study will contribute to advancement of knowledge, how the results will be utilized, not only in publications but also how they will likely affect health care, health systems, or health policies.
The link below provides more information on how to describe a research study Click here Methodology The methodology section is the most important part of the protocol. It should answer the question of why and what: It is the equivalent to the introduction in a research paper and it puts the proposal in context.
Publication policy should be clearly discussed- for example who will take the lead in publication and who will be acknowledged in publications, etc.
In the case of a randomized controlled trial additional information on the process of randomization and blinding, description of stopping rules for individuals, for part of the study or entire study, the procedures and conditions for breaking the codes etc.
Instruments which are to be used to collect information questionnaires, FGD guides, observation recording form, case report forms etc. References of literature cited in preceding sections References can also be listed at the end of Part 1.
The magnitude, frequency, affected geographical areas, ethnic and gender considerations, etc of the problem should be followed by a brief description of the most relevant studies published on the subject. If the research involves more than one group of individuals, for example healthcare users and healthcare providers, a separate specifically tailored informed consent form must be included for each group.In order to ensure your professional resume will support your goals, use this research assistant job description to inform what you should highlight on your resume.
By reviewing job description examples, you’ll be able to identify what technical and soft skills, credentials and work experience matter most to an employer in your target field. A Introduction. 3. A1. Study Abstract. 3. A2. Primary Hypothesis. 3.
Purpose of the Study Protocol. 3. B Background. 3. B1. Prior Literature and Studies. 3. B2.
Recent/Current Research: Description of research projects recently conducted or in progress. Include the type of research and a brief description of the purpose. Community Involvement: Appropriate and relevant volunteer work, church work, community service organizations, etc.
Educational Travel: Names of countries, dates, purpose. Sample resume for an entry-level research scientist A well-researched resume is vital to finding a job in the scientific field. Study this sample resume for an entry-level research scientist for ideas. Protocol title, protocol identifying number (if any), and date.
Name and address of the sponsor/funder. Name and title of the investigator(s) who is (are) responsible for conducting the research, and the address and telephone number(s) of the research site(s), including responsibilities of each. Evaluate and prepare site audits while negotiating contracts for conducting studies and research trials.
Oversee data collection, data entry and final analysis. Manage clinical trial budget, payment process, vendors and consultants. Develop clinical study protocols, plans, references and timelines.Download