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).

With several advanced clinical sites and bio-analytical laboratories in North America and India, Cliantha now has presence in 4 countries along with a strong team of 1000+ professionals. Some of the key regulators, such as the USFDA, EMA, AGES, ANSM, AMPS, MCC South Africa, Health Canada, DCGI, CAP, NABL, Turkey MOH, Thailand MoPH and others have successfully inspected Cliantha across the globe.

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 CRC, 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:

• Recruitment, screening, and coordination of patient visits as per study protocols
• Execution of all aspects of study visits as experience and training allow
• 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
• Study drug management (for outpatient dosings)
• Lab Sample processing, labelling, storage, shipment, documentation and record keeping
• IRBs interactions
• Site Regulatory Documentation collection and management
• Archiving
• 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
• Keen eye for detail, excellent organizational skills, efficient, and downright just one heck of a team player
• Good cooking/grilling/baking skills are a plus as we also love to take time to bond together as a team usually with pot lucks!
• Must be comfortable working weekends if needed

Job Type: Full-time

Pay: $46,000.00 - $54,000.00 per year

Benefits:

• 401(k)
• Dental insurance
• Flexible schedule
• Health insurance
• Paid time off
• Vision insurance

Schedule:

• 10 hour shift
• 12 hour shift
• 8 hour shift
• Day shift
• Evening shift
• Monday to Friday
• Night shift
• Weekend availability

Ability to commute/relocate:

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

Application Question(s):

• Do you have a minimum of 2 years in Clinical Research Trials Experience?

Education:

• Bachelor's (Required)

Shift availability:

• Day Shift (Required)
• Night Shift (Required)
• Overnight Shift (Required)

Work Location: One location

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