Clinical Research Associate

Join to apply for the Clinical Research Associate (90909) role at Task Impetus Inc.

As a clinical research associate (CRA) you are responsible for completing clinical research and administrative tasks for your clients. You facilitate documentation for clinical research, monitor clinical tasks for correct functioning and completion, evaluate clinical data, and create reports based on findings.

• Develop and write trial protocols (outlining purpose and methodology)
• 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 well being 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 – ensuring each centre has the trial materials, including the trial drug often known as the investigation medicinal product (IMP)
• 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 and dealing with and solving any issues
• Verify that data entered onto 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
• Meet with team members to discuss ongoing trials, results and any trends or adverse events
• 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

• University degree in scientific discipline or health care
• 2-3 years of experience in the healthcare industry, and/or clinical trials environment preferred
• Very good computer skills including MS Office
• Organisational, time management and problem‑solving skills
• Ability to establish and maintain effective working relationships with co‑workers, managers and clients

• Increment would be at least a minimum of 15% every six months.
• Relocation charges will be provided to you during your project
• Medicinal, Dental and Vision benefits following 60 days of business.
• Medical coverage qualified following 60 days of business.
• Present moment and long‑haul handicap following 60 days of work.
• 401k retirement benefits plan qualified following half a year of work.

• Employer’s Confirmation Letter/CPT Letter/Offer Letter will be provided, which you need to submit to your university within 90 days of the start of your OPT.
• OPT Extension Letter will be provided to those candidates who are qualified for STEM extension.
• H1B Sponsorship will be provided to OPT and CPT candidates only once they join our client’s project.

• Pre‑job training with experienced trainers.
• Assignments & case studies provided during training.
• Mock sessions before interviews.
• Multiple interview rounds with different clients.
• Visa sponsorship.
• Training completing certificates.

• Entry level

• Full-time

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