Associates Degree with at least 7 years' professional experience in clinical data management -OR- * High School Diploma (or equivalent) with at least 10 years' professional experience in clinical ...
New
Associates Degree with at least 7 years' professional experience in clinical data management -OR- * High School Diploma (or equivalent) with at least 10 years' professional experience in clinical ...
New
Associates Degree with at least 7 years' professional experience in clinical data management -OR- * High School Diploma (or equivalent) with at least 10 years' professional experience in clinical ...
New
Wichita, KS · On-site
Day shift | Part-time Via Christi associates are eligible for tuition discounts and priority ... Collect and analyze clinical data from diverse sources to establish a solid foundation for vital ...
Wichita, KS · On-site
Day shift | Part-time Via Christi associates are eligible for tuition discounts and priority ... Collect and analyze clinical data from diverse sources to establish a solid foundation for vital ...
Contract Senior Clinical Research Associate - Home-Based (US) ICON is a global healthcare ... Performing data review and resolution of queries to maintain high-quality clinical data.
Contract Senior Clinical Research Associate - Home-Based (US) ICON is a global healthcare ... Performing data review and resolution of queries to maintain high-quality clinical data.
Clinical Research Associate - St Louis/Kansas City/Ohio ICON plc is a world-leading healthcare ... Performing data review and resolution of queries to maintain high-quality clinical data.
Clinical Research Associate - St Louis/Kansas City/Ohio ICON plc is a world-leading healthcare ... Performing data review and resolution of queries to maintain high-quality clinical data.
Overland Park, KS · On-site
Provide electronic data capture (EDC) system training (via WebEx) for clinical research associates (CRAs) and sponsor representatives. * Lead and/or participate in user acceptance testing (UAT) for ...
Overland Park, KS · On-site
Provide electronic data capture (EDC) system training (via WebEx) for clinical research associates (CRAs) and sponsor representatives. * Lead and/or participate in user acceptance testing (UAT) for ...
... clinical data. Evaluates patient's response and intervenes to ensure optimal patient outcome ... Associate's Degree in Nursing or by endorsement * One (1) year of clinical RN experience * RN ...
New
... clinical data. Evaluates patient's response and intervenes to ensure optimal patient outcome ... Associate's Degree in Nursing or by endorsement * One (1) year of clinical RN experience * RN ...
New
In this role, you'll spearhead client events, oversee clinical data gathering, recommend clinical ... Coach, mentor and guide solution teams and new associates on recommended methodology practices and ...
In this role, you'll spearhead client events, oversee clinical data gathering, recommend clinical ... Coach, mentor and guide solution teams and new associates on recommended methodology practices and ...
Assists in providing tracking and Quality Control (QC) of data as required and assists with ... and Clinical Research Associate positions preferred * Experience in Good Clinical Practice (GCP ...
Assists in providing tracking and Quality Control (QC) of data as required and assists with ... and Clinical Research Associate positions preferred * Experience in Good Clinical Practice (GCP ...
Assists in providingtracking and Quality Control (QC) of data as required and assists with ... and Clinical Research Associate positions preferred * Experience in Good Clinical Practice (GCP ...
Assists in providingtracking and Quality Control (QC) of data as required and assists with ... and Clinical Research Associate positions preferred * Experience in Good Clinical Practice (GCP ...
Collaborating with cross-functional teams to ensure timely and accurate data collection and ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
Collaborating with cross-functional teams to ensure timely and accurate data collection and ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
Collaborating with cross-functional teams to ensure timely and accurate data collection and ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
Collaborating with cross-functional teams to ensure timely and accurate data collection and ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
Lawrence, KS · Remote
$91K - $114K/yr
We are currently seeking a Clinical Research Associate (Level II or Senior) to join our diverse and ... Performing data review and resolution of queries to maintain high-quality clinical data.
Lawrence, KS · Remote
$91K - $114K/yr
We are currently seeking a Clinical Research Associate (Level II or Senior) to join our diverse and ... Performing data review and resolution of queries to maintain high-quality clinical data.
Overland Park, KS · On-site +1
$62.25 - $82/hr
In this role, you'll spearhead client events, oversee clinical data gathering, recommend clinical ... Coach, mentor and guide solution teams and new associates on recommended methodology practices and ...
Overland Park, KS · On-site +1
$62.25 - $82/hr
In this role, you'll spearhead client events, oversee clinical data gathering, recommend clinical ... Coach, mentor and guide solution teams and new associates on recommended methodology practices and ...
$17 - $22/hr
Every associate matters and makes a difference It is truly a culture like no other - We hope you ... Verifies proper data flow conditions on the CDI network. Responds to CDI trouble calls pertaining ...
$17 - $22/hr
Every associate matters and makes a difference It is truly a culture like no other - We hope you ... Verifies proper data flow conditions on the CDI network. Responds to CDI trouble calls pertaining ...
Lenexa, KS · On-site
Clinical Organize, coordinate and lead the execution of pivotal and non-pivotal clinical studies Recruitment of clinical investigative sites Design electronic data capture (EDC) system to ensure high ...
Lenexa, KS · On-site
Clinical Organize, coordinate and lead the execution of pivotal and non-pivotal clinical studies Recruitment of clinical investigative sites Design electronic data capture (EDC) system to ensure high ...
Wichita, KS · On-site
$17 - $22/hr
Every associate matters and makes a difference It is truly a culture like no other - We hope you ... Verifies proper data flow conditions on the CDI network. Responds to CDI trouble calls pertaining ...
Wichita, KS · On-site
$17 - $22/hr
Every associate matters and makes a difference It is truly a culture like no other - We hope you ... Verifies proper data flow conditions on the CDI network. Responds to CDI trouble calls pertaining ...
$101K - $169K/yr
IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology ... data as required by the study protocol, applicable regulations and guidelines, and sponsor ...
$101K - $169K/yr
IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology ... data as required by the study protocol, applicable regulations and guidelines, and sponsor ...
$101K - $169K/yr
IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology ... data as required by the study protocol, applicable regulations and guidelines, and sponsor ...
$101K - $169K/yr
IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology ... data as required by the study protocol, applicable regulations and guidelines, and sponsor ...
Lenexa, KS · On-site
$101K - $169K/yr
IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology ... data as required by the study protocol, applicable regulations and guidelines, and sponsor ...
Lenexa, KS · On-site
$101K - $169K/yr
IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology ... data as required by the study protocol, applicable regulations and guidelines, and sponsor ...
Lenexa, KS · On-site
$101K - $169K/yr
IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology ... data as required by the study protocol, applicable regulations and guidelines, and sponsor ...
Lenexa, KS · On-site
$101K - $169K/yr
IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology ... data as required by the study protocol, applicable regulations and guidelines, and sponsor ...
$12.43 - $18.34
5% of jobs
$18.34 - $24.25
6% of jobs
$26.53 is the 25th percentile. Wages below this are outliers.
$24.25 - $30.15
35% of jobs
The median wage is $30.72 / hr.
$30.15 - $36.06
38% of jobs
$36.06 - $41.96
6% of jobs
$41.96 - $47.87
3% of jobs
$47.87 - $53.77
2% of jobs
$53.77 - $59.68
0% of jobs
$59.68 - $65.58
0% of jobs
$65.58 - $71.49
1% of jobs
$71.49 - $77.39
3% of jobs
$12
$34
$77
A clinical data associate is responsible for tracking data and results in a research study. As a clinical data associate, your job duties are to collect data, perform data management, and input data into any software used by your team. You work on a research team, so you must be able to work collaboratively and have excellent organizational skills. While you spend most of your time in an office, you may be required to work in the field to record data. The only universal qualifications needed for this career are a background in health care or medical science research and experience with data management software like Oracle Clinical, Microsoft Excel, and SPSS.
| Aspect | Clinical Data Associate | Clinical Research Coordinator |
|---|---|---|
| Primary Role | Manage and ensure accuracy of clinical trial data | Oversee trial operations, patient recruitment, and site management |
| Credentials | Bachelor's in life sciences or related field; familiarity with data management | Bachelor's in health sciences or related field; clinical trial experience |
| Work Environment | Data management teams, clinical trial databases | Clinical sites, hospitals, research facilities |
| Industry Usage | Pharmaceutical companies, CROs, biotech firms | Hospitals, research institutions, clinical trial sites |
While both roles support clinical trials, a Clinical Data Associate primarily focuses on managing and validating trial data, ensuring accuracy and compliance. In contrast, a Clinical Research Coordinator handles the overall trial operations, including patient recruitment and site coordination. Both roles require relevant certifications and work within the clinical research industry, but their daily responsibilities differ significantly.

Full-time
Medical, Dental, Vision, Retirement, PTO
Posted 2 days ago
Job Description
Principal Trial Manager (PTM)
The Principal Trial Manager is responsible for leading projects and initiatives to improve the quality and compliance of the data management functional areas in addition to the regular responsibilities as an individual Trial Manager.
Will interact with Trial Managers as SME, Mentor and Trainer within areas of expertise and provide project leadership to help develop knowledge within the department.
Will be able to work independently or as a team member or leader with equal effectiveness.
The Principal Trial Manager is responsible and accountable for the successful execution of the clinical data management strategy for one or more drug or vaccine trials within the TM role. Will be responsible for leading and/or representing data management functional areas or GDMS in cross-functional initiatives and project teams as deemed appropriate. Principle Trial Managers will possess end-to-end data management knowledge with strong project management and leadership skills which are transferable from pipeline to process to special initiatives.
Primary activities include, but are not limited to:
Lead Special Projects and Initiatives within GDMS
Act as a SME, mentor, and trainer on data management, project management, leadership and other areas of expertise
Support Training & Development programs to promote Trial Manager end-to-end proficiency
Support and provide input to the functional process owners (PO)/ potentially serving as an SME to support process implementation
Partner with functional area representatives to assess and promote consistency in the use of database standards and trial design/peer review support as needed
Identifies, defines and implements improvements to data collection, data and project management processes and tools
Support audits and inspections as necessary
Functional & cross-functional special project management
Complex Risk Management
All required activities outlined in the TM job description
Education/Experience:
Knowledge and Skills:
#MSJR
#eligibleforERP
#Clinicaltrialjob
#ONEGDMS
Required Skills:
Audit Readiness, Clinical Data Management, Communication, Cross-Functional Leadership, Data Standards, GxPs, Inspection Readiness, Mentor Coaching, Process Improvements, Project Management, Regulatory Experience, Risk ManagementPreferred Skills:
Current Employees apply HERE
Current Contingent Workers apply HERE
US and Puerto Rico Residents Only:
Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.
As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:
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We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively.
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The salary range for this role is
$142,400.00 - $224,100.00This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee's position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.
The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.
We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.
You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.
San Francisco Residents Only:We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance
Los Angeles Residents Only:We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
RegularRelocation:
No relocationVISA Sponsorship:
NoTravel Requirements:
10%Flexible Work Arrangements:
HybridShift:
1st - DayValid Driving License:
NoHazardous Material(s):
N/AJob Posting End Date:
07/16/2026*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.