Clinical Research Associate (CRA)
Job Description
Title: Clinical Research Associate (CRA)
Company Name: Bangladesh Clinical Trials Limited (a sister concern of JMI Group)
Vacancy: Not specific
Job Location: Dhaka
Employment Status: Full-time
Educational Requirements:
∎ Master of Pharmacy (M.Pharm), Master of Science (MSc) in Biochemistry, Bachelor of Medicine and Bachelor of Surgery(MBBS)
Experience Requirements:
∎ At most 2 year(s)
∎ The applicants should have experience in the following area(s):
Clinical trials, Medical Research, Quality Controller/ Assurance
∎ The applicants should have experience in the following business area(s):
Pharmaceuticals
∎ Freshers are also encouraged to apply.
Job Context:
∎ Clinical Research Associate (CRA) will responsible to run clinical trials to test drugs for it`s effectiveness, risks and benefits to ensure that these drugs are safe to allow on to the market.
∎ CRAs typically be involved in all stages of the clinical trial, including identifying an investigational site and setting up, initiating, monitoring and closing down the trial.
Job Responsibilities:
∎ Develop and write trial protocols
∎ Present trial protocols to a steering committee
∎ Design data collection forms, known as case report forms (CRFs)
∎ Coordinate with the ethics committee, which safeguards the rights, safety and wellbeing of all trial subjects
∎ Manage regulatory authority applications and approvals that oversee the research and marketing of new and existing drugs
∎ Identify and assess the suitability of facilities to use as the clinical trial site
∎ Identify/select an investigator who will be responsible for conducting the trial at the trial site
∎ Liaise with doctors, consultants or investigators on conducting the trial
∎ Set up the trial sites
∎ Train the site staff to trial-specific industry standards
∎ Monitor the trial throughout its duration, which involves visiting the trial sites on a regular basis
∎ Verify that data entered on to the CRFs is consistent with patient clinical notes, known as source data/document verification (SDV)
∎ Collect completed CRFs from hospitals and general practices
∎ Write visit reports and file and collate trial documentation and reports
∎ Ensure all unused trial supplies are accounted for
∎ Close down trial sites on completion of the trial
∎ Discuss results with a medical statistician, who writes technical trial reports
∎ Archive study documentation and correspondence
∎ Prepare final reports and occasionally manuscripts for publication
Additional Requirements:
∎ Age 23 to 32 years
∎ Both males and females are allowed to apply
∎ Should be proficient in the use of computer, e.g. MS Word, Excel, Internet, etc.
∎ Must be Fluent In English (Oral & Written)
∎ The candidate must be proactive and creative in order to formulate/implement efficient & effective business techniques.
∎ Must be proactive and creative
∎ Good interpersonal communication skills
Salary:
∎ Negotiable
∎ As per company policy
Compensation & Other Benefits:
∎ Mobile bill, Provident fund, Weekly 2 holidays, Insurance
∎ Lunch Facilities: Partially Subsidize
∎ Salary Review: Yearly
∎ Festival Bonus: 2
∎ Bangladesh Clinical Trials Ltd. offers excellent working environment, attractive compensation package and performance-based career progression to the deserving candidates.
Job Source: Bdjobs.com Online Job Posting.
Application Deadline: 17 Dec 2022
Company Information:
∎ 8 Dec 2022
∎ Bangladesh Clinical Trials Limited (a sister concern of JMI Group)
Category: Medical/Pharma
:
Source: bdjobs.com
Deadline Expired on 17th Dec 2022
More jobs of Bangladesh Clinical Trials Limited (a sister concern of JMI Group)
Clinical Research Associate (CRA), Operations
Assistant Manager, Operations
Deputy Manager/ Assistant Manager, Quality Assurance
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