Clinical Research Associate (CRA)/ Sr. CRA

Job Description

Title: Clinical Research Associate (CRA)/ Sr. CRA

Company Name: Bangladesh Clinical Trials Limited (a sister concern of JMI Group)

Vacancy: --

Age: 23 to 35 years

Job Location: Dhaka

Salary: Negotiable

Experience:

• 1 to 3 years
• The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies, Medical Equipment, Research Organization, Clinic
• Freshers are also encouraged to apply.

• Master of Pharmacy (M.Pharm)
• Master of Science (MSc) in Biochemistry
• Bachelor of Medicine and Bachelor of Surgery(MBBS)

• 1 to 3 years
• The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies, Medical Equipment, Research Organization, Clinic
• Freshers are also encouraged to apply.

• Age 23 to 35 years

• Age 23 to 35 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

Clinical Research Associate (CRA) will be responsible for running clinical trials to test drugs for their effectiveness, risks, and benefits, ensuring that these drugs are safe to be released on 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.

• 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)

• Mobile bill,Insurance,Weekly 2 holidays,Provident fund
• 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.