Our client is looking for Product data entry analyst/ sample handling support- with good Clinical ... IT Life Sciences Allied Healthcare CRO Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I Tel ...
Our client is looking for Product data entry analyst/ sample handling support- with good Clinical ... IT Life Sciences Allied Healthcare CRO Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I Tel ...
Maintain follow-up lists for pending customer master approvals, order entry, backlog changes, delivery risks, invoicing and other CRO-level exceptions. * Coordinate information and follow-up but do ...
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Maintain follow-up lists for pending customer master approvals, order entry, backlog changes, delivery risks, invoicing and other CRO-level exceptions. * Coordinate information and follow-up but do ...
Administrative Assistant III
Austin, TX · On-site
$2.9K - $3.6K/wk
EJF 1: Monitors the main CRO mailboxes daily. Screens incoming correspondence (written or ... Skill in typing from draft, data entry, proofreading, writing skills, communication and ...
Administrative Assistant III
Austin, TX · On-site
$2.9K - $3.6K/wk
EJF 1: Monitors the main CRO mailboxes daily. Screens incoming correspondence (written or ... Skill in typing from draft, data entry, proofreading, writing skills, communication and ...
Track and enable contemporaneous data entry and completeness. CRO Oversight * Oversee CRO Clinical Research Associates (CRAs) through assessment of performance, review of trends and KPIs, review of ...
Track and enable contemporaneous data entry and completeness. CRO Oversight * Oversee CRO Clinical Research Associates (CRAs) through assessment of performance, review of trends and KPIs, review of ...
Job Summary We are currently seeking an Entry Feasibility Coordinator, who will be a member of our ... Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing ...
Job Summary We are currently seeking an Entry Feasibility Coordinator, who will be a member of our ... Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing ...
Job Summary We are currently seeking an Entry Feasibility Coordinator, who will be a member of our ... Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing ...
Job Summary We are currently seeking an Entry Feasibility Coordinator, who will be a member of our ... Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing ...
The Senior CRA may also participate in monitoring oversight activities such as CRO oversight visits ... Interact with the clinical study sites to resolve data queries and/or data entry errors and obtain ...
The Senior CRA may also participate in monitoring oversight activities such as CRO oversight visits ... Interact with the clinical study sites to resolve data queries and/or data entry errors and obtain ...
The Senior CRA may also participate in monitoring oversight activities such as CRO oversight visits ... Interact with the clinical study sites to resolve data queries and/or data entry errors and obtain ...
The Senior CRA may also participate in monitoring oversight activities such as CRO oversight visits ... Interact with the clinical study sites to resolve data queries and/or data entry errors and obtain ...
... entry into study related EDC systems, contact with CRO or sponsor representatives to schedule and conduct monitoring visits as well as resolve study specific issues at the medical institution. In ...
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... entry into study related EDC systems, contact with CRO or sponsor representatives to schedule and conduct monitoring visits as well as resolve study specific issues at the medical institution. In ...
The Executive Director, Gulf Partnerships and Engagement is CARE USA's senior market-entry lead for ... Work closely with the CRO and HQ to define what CARE can commit to in partner conversations ...
The Executive Director, Gulf Partnerships and Engagement is CARE USA's senior market-entry lead for ... Work closely with the CRO and HQ to define what CARE can commit to in partner conversations ...
MO · On-site
... entry into study related EDC systems, contact with CRO or sponsor representatives to schedule and conduct monitoring visits as well as resolve study specific issues at the medical institution. In ...
Quick apply
MO · On-site
... entry into study related EDC systems, contact with CRO or sponsor representatives to schedule and conduct monitoring visits as well as resolve study specific issues at the medical institution. In ...
Clinical Trial Assistant
$75K - $90K/yr
Prepare or oversee CRO with clinical trial materials including investigator site binders, study ... Support review of data entry and reconciliation activities across systems (e.g., CTMS, eTMF, EDC ...
Clinical Trial Assistant
$75K - $90K/yr
Prepare or oversee CRO with clinical trial materials including investigator site binders, study ... Support review of data entry and reconciliation activities across systems (e.g., CTMS, eTMF, EDC ...
Clinical Trial Assistant
Foster City, CA · On-site
Prepare or oversee CRO with clinical trial materials including investigator site binders, study ... Support review of data entry and reconciliation activities across systems (e.g., CTMS, eTMF, EDC ...
Clinical Trial Assistant
Foster City, CA · On-site
Prepare or oversee CRO with clinical trial materials including investigator site binders, study ... Support review of data entry and reconciliation activities across systems (e.g., CTMS, eTMF, EDC ...
ClinChoice is a global full-service CRO with a strong focus on quality, professional development ... Develop User Acceptance Testing Plan and perform testing on data entry screens and edit checks.
ClinChoice is a global full-service CRO with a strong focus on quality, professional development ... Develop User Acceptance Testing Plan and perform testing on data entry screens and edit checks.
Create, implement and execute key sponsor / CRO strategic account activities in alignment with ... entry into Devana * Maintain current and accurate data in Devana on all leads, sales and business ...
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Create, implement and execute key sponsor / CRO strategic account activities in alignment with ... entry into Devana * Maintain current and accurate data in Devana on all leads, sales and business ...
Clinical Trial Manager
Hayward, CA · On-site
Coordinates with CRO and SMTL in clinical site oversight, data entry timeliness, assists with resolving site issues * Assists with set-up and review of clinical TMF * Organizes and manages internal ...
Clinical Trial Manager
Hayward, CA · On-site
Coordinates with CRO and SMTL in clinical site oversight, data entry timeliness, assists with resolving site issues * Assists with set-up and review of clinical TMF * Organizes and manages internal ...
Clinical Trial Manager
Brisbane, CA · On-site +1
Coordinates with CRO and SMTL in clinical site oversight, data entry timeliness, assists with resolving site issues * Assists with set-up and review of clinical TMF * Organizes and manages internal ...
Clinical Trial Manager
Brisbane, CA · On-site +1
Coordinates with CRO and SMTL in clinical site oversight, data entry timeliness, assists with resolving site issues * Assists with set-up and review of clinical TMF * Organizes and manages internal ...
... data entry screen design and testing, validation check creation, testing and approval Performs data management activities for studies conducted in-house; oversee and coordinate activities of CRO ...
... data entry screen design and testing, validation check creation, testing and approval Performs data management activities for studies conducted in-house; oversee and coordinate activities of CRO ...
Create, implement and execute key sponsor / CRO strategic account activities in alignment with ... entry into Devana * Maintain current and accurate data in Devana on all leads, sales and business ...
Create, implement and execute key sponsor / CRO strategic account activities in alignment with ... entry into Devana * Maintain current and accurate data in Devana on all leads, sales and business ...
Clinical Trial Manager
Hayward, CA · On-site +1
Coordinates with CRO and SMTL in clinical site oversight, data entry timeliness, assists with resolving site issues * Assists with set-up and review of clinical TMF * Organizes and manages internal ...
Clinical Trial Manager
Hayward, CA · On-site +1
Coordinates with CRO and SMTL in clinical site oversight, data entry timeliness, assists with resolving site issues * Assists with set-up and review of clinical TMF * Organizes and manages internal ...
Cro Entry information
See salary details
$12.26 - $13.20
2% of jobs
$13.20 - $14.14
6% of jobs
$14.14 - $15.08
6% of jobs
$16.02 is the 25th percentile. Wages below this are outliers.
$15.08 - $16.02
10% of jobs
The median wage is $16.96 / hr.
$16.02 - $16.96
25% of jobs
$16.96 - $17.90
17% of jobs
$18.73 is the 75th percentile. Wages above this are outliers.
$17.90 - $18.84
9% of jobs
$18.84 - $19.78
5% of jobs
$19.78 - $20.72
10% of jobs
$20.72 - $21.66
6% of jobs
$21.66 - $22.60
2% of jobs
$12
$17
$22
How much do cro entry jobs pay per hour?
As of Sep 13, 2026, the average hourly pay for cro entry in the United States is $17.92, according to ZipRecruiter salary data. Most workers in this role earn between $16.11 and $19.23 per hour, depending on experience, location, and employer.
What is a CRO entry?
CRO Entry jobs typically refer to entry-level positions at a Contract Research Organization (CRO). These roles often involve supporting clinical trials, data management, regulatory documentation, or assisting with research projects for pharmaceutical or biotechnology clients. Entry-level positions may include roles like Clinical Research Assistant, Data Coordinator, or Regulatory Associate. These jobs provide valuable experience for those interested in clinical research and the pharmaceutical industry, offering opportunities for career growth and skill development. Candidates usually need a bachelor’s degree in a life science or related field and strong organizational and communication skills.
What skills and qualifications are needed for a CRO entry?
To thrive as a CRO Entry-level Specialist, you need analytical thinking, a basic understanding of digital marketing principles, and familiarity with website usability concepts, often supported by a degree in marketing or a related field. Experience with tools like Google Analytics, A/B testing platforms (such as Optimizely or VWO), and basic HTML/CSS knowledge is commonly required. Strong communication, problem-solving abilities, and attention to detail help you collaborate with teams and interpret data effectively. These skills and qualifications are crucial for optimizing website performance and driving measurable business growth through data-driven decisions.
What challenges do CRO entry professionals face and how can they overcome them?
Professionals in a CRO Entry role often face challenges such as interpreting data accurately, prioritizing optimization experiments, and collaborating with cross-functional teams like design and development. It's essential to develop strong analytical skills to draw actionable insights from A/B tests and user behavior data. Effective communication and a willingness to learn from both successes and failures can help overcome these challenges, as can seeking mentorship from more experienced CRO specialists within the organization.
What is the difference between Cro Entry vs Clinical Research Coordinator?
| Aspect | Cro Entry | Clinical Research Coordinator |
|---|---|---|
| Required Credentials | High school diploma or equivalent; some roles may require basic training | Bachelor's degree in health, science, or related field; certification often preferred |
| Work Environment | Office settings, clinical sites, or research facilities | Clinical sites, hospitals, or research centers |
| Employer & Industry Usage | Pharmaceutical companies, CROs, research institutions | Hospitals, academic institutions, research organizations |
| Common Search & Comparison | Often compared for entry-level research roles | More comprehensive role involving patient interaction and data management |
In summary, Cro Entry typically requires minimal formal education and focuses on basic research support tasks, while a Clinical Research Coordinator usually holds a bachelor's degree and manages more complex aspects of clinical trials, including patient coordination and data collection.
More about Cro Entry jobs
What cities are hiring for Cro Entry jobs?
Cities with the most Cro Entry job openings:
What states have the most Cro Entry jobs?
States with the most job openings for Cro Entry jobs include:
What are popular job titles related to Cro Entry jobs?
For Cro Entry jobs, the most frequently searched job titles are:
Product data entry analyst/ sample handling support Position
Chesterfield, MO • On-site
Integrated Resources INC
• Recruiting and Staffing Services • 51 - 200 employees51 - 200 employees
Contractor
Re-posted 11 days ago
Job description
Company Description
A Few Words About Us
Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.
Job Description
Our client is looking for Product data entry analyst/ sample handling support- with good Clinical Practices, Data entry, LIMS, GMP, Data transcription / verification, and LIMS sample review experience etc.
RESPONSIBILITIES:
Data transcription, review, and trending of biologics (mAb, antibody drug conjugate, etc) stability data in preparation for regulatory filings.
Specifically, the analyst will be expected to: Retrieve data from LIMS (Laboratory Information Management System) database or other data repository.
Transcribe data into stability sections of regulatory filings, or perform 100% accuracy verification for previously transcribed data; Review sample results within LIMS to identify incomplete testing
Notify Stability Lead of any unusual findings or gaps in data; Assist Stability Leads with various tasks as necessary
Assist with sample handling duties as needed (shipment receipt, aliquoting, etc.)
Qualifications
QUALIFICATIONS AND SKILLS NEEDED:
Background in biochemistry, biology, chemistry, or related scientific discipline; Understanding of normal pharmaceutical development processes
Ability to work in a highly regulated environment and learn/comply with GMP expectations; Ability to accurately transcribe data from Excel documents to MS Word; Ability to thrive in a fast-paced environment and adapt to changing priorities; Familiar with Microsoft Office Suite, and computer literate enough to quickly learn new systems.
Additional Information
Pooja Mishra
Clinical Recruiter
Integrated Resources, Inc.
IT Life Sciences Allied Healthcare CRO
Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I
Tel: 732 429 1636
(W) 732-549-2030 x 214 | (F) 732-549-5549
Gold Seal JCAHO Certified for Health Care Staffing
"INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES" (8th Year in a Row)
About Integrated Resources
Sourced by ZipRecruiter
Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.
Industry
Recruiting and staffing services
Company size
51 - 200 Employees
Headquarters location
Edison, NJ, US
Year founded
1996