Job Details
Clinical Research Coordinator - Oxford, MS
**Clinical Research Coordinator -** **Oxford, MS**
**Work Set-Up:** On-site
**Scheduled Weekly Hours:** 16 hours per week
**Position Type:** Part-time
**About IQVIA**
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We work with top pharmaceutical, biotechnology, and medical device companies to advance patient outcomes and accelerate medical innovation. By combining scientific expertise with cutting-edge technology, IQVIA delivers high-quality clinical research that shapes the future of healthcare.
**About the Role**
IQVIA is seeking a **Clinical Research Coordinator (CRC)** to support the execution of clinical research studies at our Oxford, MS site. Under the supervision of a Principal Investigator, this role plays a critical part in patient-facing study activities, regulatory compliance, and high-quality data collection.
This is an excellent opportunity for an experienced CRC who enjoys hands-on clinical work, patient interaction, and contributing to well-conducted clinical trials in a collaborative onsite environment.
**Key Responsibilities**
+ Conduct in-person **study visits** , ensuring protocol adherence and patient safety throughout participation.
+ Perform clinical procedures including **phlebotomy, ECGs, vital signs, and specimen collection** .
+ Coordinate daily study activities, including preparation of study materials, equipment setup, and visit logistics.
+ Recruit, screen, consent, and orient study participants while maintaining a patient-centered approach.
+ Accurately collect and enter clinical data into **electronic data capture (EDC) systems** and resolve data queries.
+ Maintain compliance with study protocols, **Good Clinical Practice (GCP)** , and regulatory requirements.
+ Collaborate closely with investigators, clinical monitors, and site staff to support successful study execution.
+ Serve as a patient advocate and promote a safe, compliant clinical research environment in line with Health & Safety policies.
**Required Qualifications**
+ **Prior experience as a Clinical Research Coordinator** or in a similar clinical research role.
+ Minimum **1+ year of relevant clinical research experience** , including direct involvement in patient visits.
+ Demonstrated experience performing **phlebotomy** and other clinical procedures.
+ Working knowledge of clinical trial conduct, GCP guidelines, and medical terminology.
+ Proficiency with EDC systems, accurate data entry, and query management.
+ Strong attention to detail, organizational skills, and the ability to build effective working relationships.
**Preferred Qualifications**
+ Bachelor's degree in a science, healthcare, or related field, or an equivalent combination of education and experience.
**Additional Information**
+ This position is **not eligible for sponsorship** .
+ On-site presence in Oxford, MS is required.
+ Part-time schedule of **16 hours per week** .
**\#LI-CES #LI-DNP #LI-HCP #ONSITE**
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role is $35.00-$42.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
**Work Set-Up:** On-site
**Scheduled Weekly Hours:** 16 hours per week
**Position Type:** Part-time
**About IQVIA**
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We work with top pharmaceutical, biotechnology, and medical device companies to advance patient outcomes and accelerate medical innovation. By combining scientific expertise with cutting-edge technology, IQVIA delivers high-quality clinical research that shapes the future of healthcare.
**About the Role**
IQVIA is seeking a **Clinical Research Coordinator (CRC)** to support the execution of clinical research studies at our Oxford, MS site. Under the supervision of a Principal Investigator, this role plays a critical part in patient-facing study activities, regulatory compliance, and high-quality data collection.
This is an excellent opportunity for an experienced CRC who enjoys hands-on clinical work, patient interaction, and contributing to well-conducted clinical trials in a collaborative onsite environment.
**Key Responsibilities**
+ Conduct in-person **study visits** , ensuring protocol adherence and patient safety throughout participation.
+ Perform clinical procedures including **phlebotomy, ECGs, vital signs, and specimen collection** .
+ Coordinate daily study activities, including preparation of study materials, equipment setup, and visit logistics.
+ Recruit, screen, consent, and orient study participants while maintaining a patient-centered approach.
+ Accurately collect and enter clinical data into **electronic data capture (EDC) systems** and resolve data queries.
+ Maintain compliance with study protocols, **Good Clinical Practice (GCP)** , and regulatory requirements.
+ Collaborate closely with investigators, clinical monitors, and site staff to support successful study execution.
+ Serve as a patient advocate and promote a safe, compliant clinical research environment in line with Health & Safety policies.
**Required Qualifications**
+ **Prior experience as a Clinical Research Coordinator** or in a similar clinical research role.
+ Minimum **1+ year of relevant clinical research experience** , including direct involvement in patient visits.
+ Demonstrated experience performing **phlebotomy** and other clinical procedures.
+ Working knowledge of clinical trial conduct, GCP guidelines, and medical terminology.
+ Proficiency with EDC systems, accurate data entry, and query management.
+ Strong attention to detail, organizational skills, and the ability to build effective working relationships.
**Preferred Qualifications**
+ Bachelor's degree in a science, healthcare, or related field, or an equivalent combination of education and experience.
**Additional Information**
+ This position is **not eligible for sponsorship** .
+ On-site presence in Oxford, MS is required.
+ Part-time schedule of **16 hours per week** .
**\#LI-CES #LI-DNP #LI-HCP #ONSITE**
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role is $35.00-$42.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
Job #NLX290694939