Clinical Research Coordinator
$35 - $42/hr
On-site Schedule: Part-time, 24 hours per week About the Role We are seeking a Clinical Research ... About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical ...
Clinical Research Coordinator
$35 - $42/hr
On-site Schedule: Part-time, 24 hours per week About the Role We are seeking a Clinical Research ... About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical ...
On-site Schedule: Part-time, 24 hours per week About the Role We are seeking a Clinical Research ... About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical ...
On-site Schedule: Part-time, 24 hours per week About the Role We are seeking a Clinical Research ... About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical ...
Clinical Research Coordinator - Germantown, TN
Germantown, TN · On-site
$35 - $42/hr
On-site Schedule: Part-time, 24 hours per week About the Role We are seeking a Clinical Research ... About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical ...
Clinical Research Coordinator - Germantown, TN
Germantown, TN · On-site
$35 - $42/hr
On-site Schedule: Part-time, 24 hours per week About the Role We are seeking a Clinical Research ... About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical ...
... Allscripts Electronic Health Record as required for reporting tests and communicating with ... Complete any paperwork required. • Must have good analytical judgment. • Ability to work under ...
... Allscripts Electronic Health Record as required for reporting tests and communicating with ... Complete any paperwork required. • Must have good analytical judgment. • Ability to work under ...
Utilize Allscripts Electronic Health Record as required for reporting tests and communicating with ... Must have good analytical judgment. Ability to work under pressure, strong problem-solving skill ...
Utilize Allscripts Electronic Health Record as required for reporting tests and communicating with ... Must have good analytical judgment. Ability to work under pressure, strong problem-solving skill ...
Part Time Allscripts Analyst information
See salary details
$29.5K - $38K
0% of jobs
$38K - $46.5K
12% of jobs
$54.2K is the 25th percentile. Wages below this are outliers.
$46.5K - $55K
15% of jobs
$55K - $63.5K
18% of jobs
The median wage is $65.6K / yr.
$63.5K - $72K
23% of jobs
$76.7K is the 75th percentile. Wages above this are outliers.
$72K - $80.5K
14% of jobs
$80.5K - $89K
4% of jobs
$89K - $97.5K
3% of jobs
$97.5K - $106K
7% of jobs
$106K - $114.5K
2% of jobs
$114.5K - $123K
2% of jobs
$29.5K
$71.5K
$123K
How much do part time allscripts analyst jobs pay per year?
As of Jun 21, 2026, the average yearly pay for part time allscripts analyst in the United States is $71,511.00, according to ZipRecruiter salary data. Most workers in this role earn between $54,500.00 and $79,000.00 per year, depending on experience, location, and employer.
What are the most commonly searched types of Allscripts Analyst jobs? The most popular types of Allscripts Analyst jobs are:
$35 - $42/hr
Part-time
Medical, Life
Posted 24 days ago
IQVIA rating
8.2
Based on 52 frontline employees who took The Breakroom Quiz
45th of 204 rated it services
Job description
Clinical Research Coordinator - Germantown, TN
Work Set-Up: On-site
Schedule: Part-time, 24 hours per weekAbout the RoleWe are seeking a Clinical Research Coordinator (CRC) to join our team and support clinical research studies under the supervision of a principal investigator. This role involves hands-on clinical procedures, community outreach, and ensuring the highest standards of care and compliance. Responsibilities also include working directly with consenting patients, conducting study visits, processing laboratory samples, and performing ambulatory blood pressure monitor (ABPM) procedures. Accurate and timely data entry will be an essential part of this role.About IQVIAIQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world's leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials.Key Responsibilities
Work Set-Up: On-site
Schedule: Part-time, 24 hours per weekAbout the RoleWe are seeking a Clinical Research Coordinator (CRC) to join our team and support clinical research studies under the supervision of a principal investigator. This role involves hands-on clinical procedures, community outreach, and ensuring the highest standards of care and compliance. Responsibilities also include working directly with consenting patients, conducting study visits, processing laboratory samples, and performing ambulatory blood pressure monitor (ABPM) procedures. Accurate and timely data entry will be an essential part of this role.About IQVIAIQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world's leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials.Key Responsibilities
- Perform a variety of complex clinical procedures, including ECG, spirometry, sample collection, and vital signs.
- Phlebotomy is required; pediatric experience is highly preferred.
- Coordinate clinical research studies and maintain compliance with protocols and Good Clinical Practice (GCP) guidelines.
- Conduct patient consenting and perform study visits in accordance with study protocols.
- Process laboratory samples and perform ABPM (ambulatory blood pressure monitor) procedures.
- Support study conduct by preparing study materials, setting up equipment, and planning logistical activities.
- Recruit, screen, and orient volunteers, ensuring their safety and well-being throughout the study.
- Collect and accurately record clinical data in case report forms (CRFs); complete timely and highquality data entry.
- Collaborate with investigators and monitors, addressing queries and ensuring data quality.
- Act as a volunteer advocate and maintain a safe environment in accordance with Health and Safety policies.
- High School Diploma or equivalent education and experience.
- Minimum 1 year of relevant work experience in clinical research (preferred).
- Working knowledge of clinical trials, GCP principles, and medical terminology.
- Strong attention to detail and ability to establish effective working relationships.
- Experience with CRIO is a plus.
- Experience with Allscripts/Altera EMR is a plus.
#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 athttps://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.
About IQVIA
Sourced by ZipRecruiter
At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.
Industry
Health care and social assistance
Company size
10,000+ Employees
Headquarters location
Durham, NC, US