Clinical Assistant (Clinical Trials)
About the role
INSTRUCTION TO APPLY; PLEASE APPLY ACCORDINGLY OR YOUR APPLICATION WILL NOT BE ACCEPTED:
When you click on Apply Now, please ensure you attach your PDF resume. Indeed Resumes will not be considered. Click on “Apply with a different resume” and attach your PDF resume there. DO NOT attach Word format resumes.
Cliantha is currently seeking Clinical Assistant(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 (Florida & New Jersey)& Canada (Mississauga & Scarborough).
General Responsibilities:
- Participate in the selection of subject’s for clinical trial through the screening process and or required during the conduct of the study. Duties may include but are not limited to:
- Obtaining ECG’s
- Obtaining Vital signs (blood pressure, temperature, pulse oximetry, respiration rate)
- Performing a subject interview
- Processing of blood and urines samples as per protocol requirements
- Perform in-house screening diagnostics such as Drug Screen panels, pregnancy tests, cotinine tests, alcohol breathalyzer tests, etc.
- Documenting and packaging of study samples for shipment to the appropriate clinical diagnostic or analytical laboratory
- Obtaining subject’s height, weight, elbow breadth, frame size and body mass index
- Study related tasks such as meals (distribution, collection and monitoring), subject assembly, check in procedures, property room, etc.
- Monitor subjects during in-house confinement periods for protocol and SOP requirement such as physical restrictions, water restrictions, meals, fluid intake/output, etc.
- Preparation of study related materials, such as labelling of study tubes, preparation of clipboards, ensuring clinic is prepared with supplies required
- Review study documents for completeness and accuracy and ensure all corrections are followed up with promptly
- Ensure personal resume (CV) is updated annually as required.
- May be required to keep personal training file updated on a regular basis.
- Participate in training sessions.
- Work in a safe manner that does not endanger yourself or your co-workers.
- Execute other duties as may be required by their manager and other members of Inflamax
- Research Management team as training and experience allow.
- Assist in development of department SOPs, Equipment Binders, templates
- Procurement of equipment and supplies as required
- Calibration and maintenance of equipment per SOPs; Maintain appropriate logbooks
- Participate in training of staff as experience and qualifications permit
- Uphold the company mission statement and conduct yourself at all times in a respectful and business-like manner. Be a positive role model for all staff and interact with colleagues in a collaborative way
- Assist in set up and maintenance of laboratory
- Execute other duties as may be required
Qualifications:
- Grade 12 education or equivalent
- 0-1 year experience in a basic laboratory setting
- Clinical experience; preferably in a CRO or Pharmaceutical setting, would be an asset
- Recognized professional certification in clinical research would be an asset
- Reliability and flexibility with availability for shifts
- Excellent organizational skills, detail oriented, efficient and able to multi-task and prioritize effectively
- Strong analytical and problem solving skills
- Excellent organizational skills, detail oriented, efficient and able to multi-task 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.
We thank all our candidates for taking interest and the time to apply for stated job vacancy; however only those selected will be contacted for next steps.
Job Type: Permanent
Pay: $18.00-$21.00 per hour
Work Location: In person
About Cliantha Research Limited
Cliantha Research, a full-service Clinical Research Organization (CRO), is a leading provider of Clinical research services, based in Ahmedabad, India. Cliantha’s mission is Science with Integrity. Cliantha has fifteen years of impeccable regulatory history with USFDA, WHO, MHRA, Health Canada, AGES, AEMPS, MCC, MOH, ANSM, MOPH, ANVISA, CAP, and NABL.
Clinical Assistant (Clinical Trials)
About the role
INSTRUCTION TO APPLY; PLEASE APPLY ACCORDINGLY OR YOUR APPLICATION WILL NOT BE ACCEPTED:
When you click on Apply Now, please ensure you attach your PDF resume. Indeed Resumes will not be considered. Click on “Apply with a different resume” and attach your PDF resume there. DO NOT attach Word format resumes.
Cliantha is currently seeking Clinical Assistant(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 (Florida & New Jersey)& Canada (Mississauga & Scarborough).
General Responsibilities:
- Participate in the selection of subject’s for clinical trial through the screening process and or required during the conduct of the study. Duties may include but are not limited to:
- Obtaining ECG’s
- Obtaining Vital signs (blood pressure, temperature, pulse oximetry, respiration rate)
- Performing a subject interview
- Processing of blood and urines samples as per protocol requirements
- Perform in-house screening diagnostics such as Drug Screen panels, pregnancy tests, cotinine tests, alcohol breathalyzer tests, etc.
- Documenting and packaging of study samples for shipment to the appropriate clinical diagnostic or analytical laboratory
- Obtaining subject’s height, weight, elbow breadth, frame size and body mass index
- Study related tasks such as meals (distribution, collection and monitoring), subject assembly, check in procedures, property room, etc.
- Monitor subjects during in-house confinement periods for protocol and SOP requirement such as physical restrictions, water restrictions, meals, fluid intake/output, etc.
- Preparation of study related materials, such as labelling of study tubes, preparation of clipboards, ensuring clinic is prepared with supplies required
- Review study documents for completeness and accuracy and ensure all corrections are followed up with promptly
- Ensure personal resume (CV) is updated annually as required.
- May be required to keep personal training file updated on a regular basis.
- Participate in training sessions.
- Work in a safe manner that does not endanger yourself or your co-workers.
- Execute other duties as may be required by their manager and other members of Inflamax
- Research Management team as training and experience allow.
- Assist in development of department SOPs, Equipment Binders, templates
- Procurement of equipment and supplies as required
- Calibration and maintenance of equipment per SOPs; Maintain appropriate logbooks
- Participate in training of staff as experience and qualifications permit
- Uphold the company mission statement and conduct yourself at all times in a respectful and business-like manner. Be a positive role model for all staff and interact with colleagues in a collaborative way
- Assist in set up and maintenance of laboratory
- Execute other duties as may be required
Qualifications:
- Grade 12 education or equivalent
- 0-1 year experience in a basic laboratory setting
- Clinical experience; preferably in a CRO or Pharmaceutical setting, would be an asset
- Recognized professional certification in clinical research would be an asset
- Reliability and flexibility with availability for shifts
- Excellent organizational skills, detail oriented, efficient and able to multi-task and prioritize effectively
- Strong analytical and problem solving skills
- Excellent organizational skills, detail oriented, efficient and able to multi-task 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.
We thank all our candidates for taking interest and the time to apply for stated job vacancy; however only those selected will be contacted for next steps.
Job Type: Permanent
Pay: $18.00-$21.00 per hour
Work Location: In person
About Cliantha Research Limited
Cliantha Research, a full-service Clinical Research Organization (CRO), is a leading provider of Clinical research services, based in Ahmedabad, India. Cliantha’s mission is Science with Integrity. Cliantha has fifteen years of impeccable regulatory history with USFDA, WHO, MHRA, Health Canada, AGES, AEMPS, MCC, MOH, ANSM, MOPH, ANVISA, CAP, and NABL.