Research Associate
Job Description
Title: Research Associate
Company Name: Association for Community Empowerment-ACE
Vacancy: 01
Job Location: Dhaka
Employment Status: Full-time, Contractual
Educational Requirements:
∎ Master's degree from any recognize university / tertiary educational qualifications in a clinical or life sciences related field (relevant experience/qualifications in similar professions may also be considered).
∎ Skills Required: Database Application, Google drive, google work space, Microsoft Excel, MICROSOFT OFFICE, Microsoft PowerPoint, outlook
Experience Requirements:
∎ 4 to 5 year(s)
∎ The applicants should have experience in the following area(s):
clinical research center, clinical trial coordination, dissemination of research outcomes, patient interaction, Protocol development, public health, Qualitative research, Research and Development
Job Responsibilities:
∎ Acting as key contact to ensure that studies are conducted and documented per guidelines and local/global regulatory requirements. Coordinates with the Head of Longitudinal Research of CSUR and the Head of Research of ACE to help ensure that clinical research protocol development and related activities are performed in accordance with research proposal, policies and procedures.
∎ Assists the research team leader and other research fellows in the development of materials and tools necessary to conduct the study around issues related to (but not limited to) protocol requirements, schedule of visits, and execution of the research plan.
∎ Reviews and comprehends the protocol, Attends meetings as required or requested by the team leader.
∎ Prepares other study materials as requested by the research team leader. These study materials include, but are not limited to, the informed consent document; case report forms (CRFs), enrolment logs, and drug/device accountability logs.
∎ Collecting, processing and analysing data; literature review & develop literature search strategy.
∎ Screens subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant's eligibility or exclusion. Establishes and organizes study files, including but not limited to, regulatory binders, study specific source documentation and other materials.
∎ Reviews and develops a familiarity with the protocol, e.g., study proceedings and timelines, inclusion and exclusion criteria, confidentiality, privacy protections.
∎ Assists research team in communication of study requirements to the stakeholders. Conducts or participates in the informed consent process and discussions with research participants, including answering any questions related to the study.
∎ Completes study documentation, disseminations and maintains study files in accordance with project requirements, policies and procedures including, but not limited to, consent forms, source documentation, narrative notes if applicable, case report forms, and investigational material accountability forms.
Additional Requirements:
∎ Minimum 4-5 years of solid research experience.
∎ Prior experience or knowledge of literature review with a systematic approach in the context of scientific studies.
∎ Sound understanding of research methodologies and good record of publication.
∎ Strong statistical and mathematical aptitude (Expertise in R/SPSS/STATA or other statistical software is required).
∎ Expertise in RCT (Randomized Controlled Trial) will be an added advantage.
∎ Advanced oral, written, and interpersonal communication skills to enable engagement with a variety of stakeholders.
∎ Demonstrated initiative and ability to work effectively autonomously and within a team environment.
∎ Proven proficiency in the use of the Microsoft Office suite including Word, Excel, PowerPoint, and Outlook, as well as database applications.
∎ Ability to adapt to a fast-paced environment and be flexible with work hours.
∎ Well-developed organizational and problem-solving skills to ensure smooth workflow and meeting deadlines.
∎ Extensive knowledge of clinical trial monitoring procedures, and medical terminology are essential
∎ Experience in the preparation of regulatory submissions and correspondence, and safety reporting
∎ Monitoring all aspects of studies to ensure compliance with study protocol and regulatory requirements, and preparation of monitoring reports
Salary: Tk. 90000 - 100000 (Monthly)
Compensation & Other Benefits:
∎ Lunch Facilities: Partially Subsidize
∎ The position will be effective from 1 November 2022.
Job Source: Bdjobs.com Online Job Posting.
Application Deadline: 16 Oct 2022
Company Information:
∎ 11 Oct 2022
∎ Association for Community Empowerment-ACE
∎ Address : Flat: A-6, House no.: 6/11, Block: E, Lalmatia, Dhaka-1207, Bangladesh
∎ Web : https://ace.org.bd/
∎ Business : Association for Community Empowerment-ACE is a non-profit organization, founded in 2020 and registered in 2021 under the Ministry of Social Welfare of Bangladesh. ACE was initiated by a collective force of development professionals with a shared vision to empower underprivileged communities and individuals with proper skills and actions. We are determined to enhance community advancement, and contribute to sustainable development. We address the nation’s most demanding issues including women empowerment, capacity building, health and nutrition, meaningful economic empowerment, quality education, youth development, and environmental protection. ACE works for people of all races, religions, and nationalities to partner in its mission. We find the best way to deliver innovative programs that change behaviors, transmit individual energy and empathy in creating evidence for social good.
Category: NGO/Development
: This is a full-time contractual position, initially for 8 months, if you are interested in applying for this position, please include a CV and cover letter with your application, mentioning the name of the position "Research Associate" in the subject line. The position will be effective from 1 November 2022.
Deadline Expired on 16th Oct 2022
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