Clinical Research Coordinator - Mississauga, Canada - Cliantha Research Ltd.

Cliantha Research Ltd.

Verified Company

Mississauga, Canada

1 week ago

Posted by:

Sophia Lee

beBee Recruiter

Description

_Cliantha Research Inc._ is currently seeking Part-Time Clinical Research Coordinator(s) who can fulfill its business needs and is looking for better learning and growth opportunities.

About Us

Cliantha Research is a full service Clinical Research Organization (CRO) that provides comprehensive and integrated offerings in Early Phase, Late Phase, Respiratory, Tobacco Research, 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, Canada, and Europe.

General responsibilities:

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 mínimal 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 Regulator 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 Kickoff meetings and regular study update meetings

Qualifications:

B.Sc., postsecondary 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 Ph14 studies, EEC is desirable
Good troubleshooting and decision making skills, able to escalate response to situations when relevant
Proven solid project planning/coordination/management skills
Strong analytical and problem solving skills
Excellent organizational skills, detail oriented, efficient and able to multitask and prioritize effectively
Excellent interpersonal skills
Strong written and verbal communication skills
Cliantha Research is committed to creating and maintaining a diverse, inclusive, and accessible environment for all its employees and clients. We value diversity at workplace and believe in fostering a spirit of excellence brought in by all our employees and clients. If you require accommodation before, during, or after the interview/recruitment process do not hesitate to let us know when we contact you and we will work with you and do our level best to meet your needs._

Job Types:
Part-time, Permanent

Schedule: