Job description

ABOUT CLIANTHA

Cliantha Research is one of the fastest growing Clinical Research Organization (CRO) in north America, stemming from our decades of experience in Asia and Europe.

We provide comprehensive and integrated offerings in Early Phase, Late Phase, Respiratory, Dermatology, Consumer Research, Research Lab, IVRT, Biometrics, Pharmacovigilance & Medical Services, and Environmental Exposure Chambers (EECs).

Cliantha Research is headquartered in Ahmedabad and has expanded its domestic presence with 5 regional offices & international presence with offices in USA (Florida), Canada (Mississauga, Winnipeg & Scarborough) & Europe (Portugal).

WHAT YOU WILL BE DOING:

This is a key role in the success of our organization, and as a Research Assistant, your main function is to assist in the overall conduct of clinical studies for BE and Phase 1-4 studies including but not limited to:

• Conducts clinical procedures and assist investigators with patient screening, enrollment, interim visits and final visits
• Assesses subjects’ protocol and medication compliance and documents adverse events including follow-up with subjects
• Perform clinical and study procedures as per study protocols, ensuring minimal deviations and proper tracking and reporting when deviations occur
• Interact with Principal Investigator, sponsor, manager and Scientific Director and other study coordinators to ensure all aspects of protocols and study requirements are understood
• Assist in design, implementation and coordination of all aspects of data collection, source documentation and CRF transcription as per protocol, SOPs and ICH/GCP guidelines
• Data entry as required
• Participate in development and execution of Quality Control processes
• Prepare for and support QA audits and sponsor monitoring visits
• Lab Sample processing, labelling, storage, shipment, documentation and record keeping
• Work with study managers and other members of the study teams to ensure study performance meets or exceeds client expectations
• Participate in Operational kick-off meetings and regular study update meetings
• Ensure study subjects are having the best possible experience while participating in studies

WHAT YOU MUST BRING TO BE THE SUPERHERO WE NEED:

• B.Sc., post-secondary diploma in scientific, healthcare or pharmaceutical field, or equivalent experience and/or education.
• Minimum 2 years’ experience in a clinical research environment preferably including BE and Ph 1 – IV studies, EEC is desirable
• Phlebotomy skills is essential
• Keen eye for detail, excellent organizational skills, efficient, and downright just one heck of a team player
• Able to work weekends and overnight when studies dictate
• Bi-lingual applicants encourage to apply

Job Types: Full-time, Part-time

Pay: $14.00 - $19.00 per hour

Schedule:

• 10 hour shift
• 4 hour shift
• 8 hour shift

Ability to commute/relocate:

• Saint Petersburg, FL 33714: Reliably commute or planning to relocate before starting work (Required)

Experience:

• Phlebotomy: 1 year (Required)
• Clinical trials: 2 years (Required)

Work Location: One location

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