... how we work and interact with each other, customers, patients and suppliers. We are currently ... Your role will extend beyond the clinical aspects as you chaperone study subjects during their ...
... how we work and interact with each other, customers, patients and suppliers. We are currently ... Your role will extend beyond the clinical aspects as you chaperone study subjects during their ...
Regulatory Associate
Overland Park, KS · On-site
At Altasciences we all move in unison to assist and work in the discovery, development, and ... Ensuring all documentation is in place for the applicable clinical studies, Investigators ...
Regulatory Associate
Overland Park, KS · On-site
At Altasciences we all move in unison to assist and work in the discovery, development, and ... Ensuring all documentation is in place for the applicable clinical studies, Investigators ...
Your role will extend beyond the clinical aspects as you chaperone study subjects during their ... equivalent work experience in a similar role, we want to hear from you. * 1+ years of work ...
Your role will extend beyond the clinical aspects as you chaperone study subjects during their ... equivalent work experience in a similar role, we want to hear from you. * 1+ years of work ...
Your role will extend beyond the clinical aspects as you chaperone study subjects during their ... equivalent work experience in a similar role, we want to hear from you. * 1+ years of work ...
Your role will extend beyond the clinical aspects as you chaperone study subjects during their ... equivalent work experience in a similar role, we want to hear from you. * 1+ years of work ...
Payroll/Human Resources Specialist
Dodge City, KS · On-site
$17.50 - $18/hr
Oversee student work-study applications, paperwork, and onboarding. * Prepare and provide reports ... Associates degree or certificate * Two years of computerized accounts receivable or accounts ...
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Payroll/Human Resources Specialist
Dodge City, KS · On-site
$17.50 - $18/hr
Oversee student work-study applications, paperwork, and onboarding. * Prepare and provide reports ... Associates degree or certificate * Two years of computerized accounts receivable or accounts ...
Student Employment (non Work Study) Position: Student Media Center Department: Student Success & Engagement Type of Position: Student employee Exemption Status: Non-Exempt Work Schedule, Hours per ...
Student Employment (non Work Study) Position: Student Media Center Department: Student Success & Engagement Type of Position: Student employee Exemption Status: Non-Exempt Work Schedule, Hours per ...
Sr. Clinical Research Associate, IQVIA
$101.60K - $169.30K/yr
IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology ... Perform monitoring and site management work to ensure that sites are conducting the study(ies) and ...
Sr. Clinical Research Associate, IQVIA
$101.60K - $169.30K/yr
IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology ... Perform monitoring and site management work to ensure that sites are conducting the study(ies) and ...
Sr. Clinical Research Associate, IQVIA
$101.60K - $169.30K/yr
IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology ... Perform monitoring and site management work to ensure that sites are conducting the study(ies) and ...
Sr. Clinical Research Associate, IQVIA
$101.60K - $169.30K/yr
IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology ... Perform monitoring and site management work to ensure that sites are conducting the study(ies) and ...
Sr. Clinical Research Associate, IQVIA
Overland Park, KS · On-site
$101.60K - $169.30K/yr
IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology ... Perform monitoring and site management work to ensure that sites are conducting the study(ies) and ...
Sr. Clinical Research Associate, IQVIA
Overland Park, KS · On-site
$101.60K - $169.30K/yr
IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology ... Perform monitoring and site management work to ensure that sites are conducting the study(ies) and ...
Sr. Clinical Research Associate, IQVIA
$101.60K - $169.30K/yr
IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology ... Perform monitoring and site management work to ensure that sites are conducting the study(ies) and ...
Sr. Clinical Research Associate, IQVIA
$101.60K - $169.30K/yr
IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology ... Perform monitoring and site management work to ensure that sites are conducting the study(ies) and ...
Your role will involve delivering clinical research operations work to a high standard, working ... Your role will extend beyond the clinical aspects as you chaperone study subjects during their ...
Your role will involve delivering clinical research operations work to a high standard, working ... Your role will extend beyond the clinical aspects as you chaperone study subjects during their ...
Administrative Assistant to School of Arts and Sciences
Wichita, KS · On-site
$16.25 - $21.75/hr
Supervise work-study students, including timesheet coordination and maintaining salary expenditure ... High school diploma required; associate or bachelor's degree preferred. * Must be legally ...
Administrative Assistant to School of Arts and Sciences
Wichita, KS · On-site
$16.25 - $21.75/hr
Supervise work-study students, including timesheet coordination and maintaining salary expenditure ... High school diploma required; associate or bachelor's degree preferred. * Must be legally ...
Your role will involve delivering clinical research operations work to a high standard, working ... Your role will extend beyond the clinical aspects as you chaperone study subjects during their ...
Your role will involve delivering clinical research operations work to a high standard, working ... Your role will extend beyond the clinical aspects as you chaperone study subjects during their ...
Your role will involve delivering clinical research operations work to a high standard, working ... Your role will extend beyond the clinical aspects as you chaperone study subjects during their ...
Your role will involve delivering clinical research operations work to a high standard, working ... Your role will extend beyond the clinical aspects as you chaperone study subjects during their ...
Collaborating with investigators and site staff to facilitate smooth study conduct. * Performing ... Ability to work independently and collaboratively in a fast-paced environment. * Ability to travel ...
Collaborating with investigators and site staff to facilitate smooth study conduct. * Performing ... Ability to work independently and collaboratively in a fast-paced environment. * Ability to travel ...
Associate Director, Oncology Epidemiology
Wichita, KS · On-site +1
The Associate Director, Oncology Epidemiology role is accountable for working independently, and in ... with study design; and identify and evaluate data resources to meet therapeutic needs. * Work ...
Associate Director, Oncology Epidemiology
Wichita, KS · On-site +1
The Associate Director, Oncology Epidemiology role is accountable for working independently, and in ... with study design; and identify and evaluate data resources to meet therapeutic needs. * Work ...
Associate Director, Oncology Epidemiology
Topeka, KS · On-site +1
The Associate Director, Oncology Epidemiology role is accountable for working independently, and in ... with study design; and identify and evaluate data resources to meet therapeutic needs. * Work ...
Associate Director, Oncology Epidemiology
Topeka, KS · On-site +1
The Associate Director, Oncology Epidemiology role is accountable for working independently, and in ... with study design; and identify and evaluate data resources to meet therapeutic needs. * Work ...
Associate Director, Oncology Epidemiology
Kansas City, KS · On-site +1
The Associate Director, Oncology Epidemiology role is accountable for working independently, and in ... with study design; and identify and evaluate data resources to meet therapeutic needs. * Work ...
Associate Director, Oncology Epidemiology
Kansas City, KS · On-site +1
The Associate Director, Oncology Epidemiology role is accountable for working independently, and in ... with study design; and identify and evaluate data resources to meet therapeutic needs. * Work ...
The Associate Director, Oncology Epidemiology role is accountable for working independently, and in ... with study design; and identify and evaluate data resources to meet therapeutic needs. * Work ...
The Associate Director, Oncology Epidemiology role is accountable for working independently, and in ... with study design; and identify and evaluate data resources to meet therapeutic needs. * Work ...
Associate Director, Oncology Epidemiology
Pittsburg, KS · On-site +1
The Associate Director, Oncology Epidemiology role is accountable for working independently, and in ... with study design; and identify and evaluate data resources to meet therapeutic needs. * Work ...
Associate Director, Oncology Epidemiology
Pittsburg, KS · On-site +1
The Associate Director, Oncology Epidemiology role is accountable for working independently, and in ... with study design; and identify and evaluate data resources to meet therapeutic needs. * Work ...
Work Study Associate information
Other
Medical, Dental, Vision, Life, Retirement
Posted 4 days ago
Job description
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
We are currently seeking a Medical Research Associate (Phlebotomist) to join our diverse and dynamic team.
As a Medical Research Associate at ICON, you will be responsible for meeting/greeting clinical research volunteers as they come into the clinic, checking their vitals (height, weight, blood pressure, BMI), and essentially making sure the study participants are healthy enough to participate in the clinical trial according to the protocol of a study.
What you will be doing
- Your compassion and dedication will be at the forefront as you take vital signs and perform phlebotomy on study subjects, ensuring their comfort and well-being throughout the research process.
- You will be entrusted with following our clients' protocols when conducting vital sign assessments and phlebotomy procedures.
- Joining us means being part of a collaborative environment where your active participation in meetings and other assignments will be valued and recognized.
- Your role will extend beyond the clinical aspects as you chaperone study subjects during their breaks outside, offering personalized care and ensuring their comfort.
Your profile
- A strong command of both English and the host country's language is essential, enabling effective communication and collaboration.
- A High School Diploma or G.E.D. qualification
- If you possess an undergraduate degree in a clinical or health-related area, or have equivalent work experience in a similar role, we want to hear from you.
- 1+ years of work experience in a medical or clinical field is preferred
- If you hold certifications such as Basic Life Support (BLS) or Phlebotomist Certification, it will be a great advantage
- Preferred Background: Medical Assistant, Certified Nursing Assistant, Certified Medication Aide, Telemetry Technician, or Laboratory Technician backgrounds are highly desired
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.