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Cro Entry Jobs (NOW HIRING)

PSI CRO

... 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 ...

PSI CRO

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 ...

Evolution Research Group

Data Entry Clerk

Columbus, OH · On-site

$16 - $21.25/hr

Data Entry Coordinator/Clerk Location: About Company: Who is ERG? ERG is a leading U.S. based ... With CRC and/or manager oversight assist Sponsor or CRO data manager with resolution of queries to ...

Evolution Research Group

Data Entry Clerk

Columbus, OH · On-site

$16.50 - $22/hr

Data Entry Coordinator/Clerk Location: About Company: Who is ERG? ERG is a leading U.S. based ... With CRC and/or manager oversight assist Sponsor or CRO data manager with resolution of queries to ...

Quotient Sciences

Data Entry Coordinator

Miami, FL · On-site

... and Clinical (CRO) services across the entire development pathway, including formulation ... Responsible for the following data entry associated tasks for their assigned studies: source ...

VALENCIA GROUP

Reservations Agent- CRO

San Antonio, TX · On-site

$16/hr

... entry, communication, and collaboration with internal teams. The role also provides cross ... Support Collaborative Revenue Optimization (CRO) initiatives by assisting with special projects as ...

VALENCIA GROUP

Reservations Agent- CRO

San Antonio, TX · On-site

$14.50 - $18/hr

... entry, communication, and collaboration with internal teams. The role also provides cross ... Support Collaborative Revenue Optimization (CRO) initiatives by assisting with special projects as ...

Valencia Group

Reservations Agent- CRO

San Antonio, TX · On-site

$14.50 - $18.25/hr

... entry, communication, and collaboration with internal teams. The role also provides cross ... Support Collaborative Revenue Optimization (CRO) initiatives by assisting with special projects as ...

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Cro Entry information

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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?

AspectCro EntryClinical Research Coordinator
Required CredentialsHigh school diploma or equivalent; some roles may require basic trainingBachelor's degree in health, science, or related field; certification often preferred
Work EnvironmentOffice settings, clinical sites, or research facilitiesClinical sites, hospitals, or research centers
Employer & Industry UsagePharmaceutical companies, CROs, research institutionsHospitals, academic institutions, research organizations
Common Search & ComparisonOften compared for entry-level research rolesMore 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?

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What states have the most Cro Entry jobs?

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What are popular job titles related to Cro Entry jobs?

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Cro Entry jobs near you
Infographic showing various Cro Entry job openings in the United States as of September 2026, with employment types broken down into 63% Full Time, 36% Part Time, and 1% Contract. Highlights an 41% Physical, 2% Hybrid, and 57% Remote job distribution, with an average salary of $37,275 per year, or $17.9 per hour.

Data Entry Coordinator

Charlotte, NC • On-site

Joint and Muscle Medical Care
See more jobs at Joint and Muscle Medical Careexternal

Other

Medical, PTO

Re-posted 15 days ago

Job description

Benefits:
  • Health insurance
  • Opportunity for advancement
  • Paid time off
  • Training & development
Clinical Research Data Entry Coordinator - Job Description Summary

The Clinical Research Data Entry Coordinator supports clinical trials by ensuring timely, accurate, and compliant entry of study data into electronic data capture (EDC) systems. This role works closely with study coordinators, investigators, and monitors to maintain high-quality documentation and uphold regulatory standards across all assigned studies.

Key Responsibilities
  • Data Entry & Verification — Enter source data into EDC systems (e.g., Medidata Rave, REDCap, Inform) with high accuracy; perform ongoing data cleaning and query resolution.
  • Source Documentation Review — Compare source documents against EDC entries to ensure consistency and completeness.
  • Query Management — Respond to data queries from sponsors/CROs within required timelines; collaborate with clinical staff to obtain missing information.
  • Regulatory Compliance — Maintain adherence to GCP, ICH guidelines, and site SOPs; ensure audit-ready documentation.
  • Study Support — Assist coordinators with visit documentation, data reconciliation, and tracking of study milestones.
  • Data Quality Assurance — Conduct periodic data reviews, identify trends or recurring issues, and elevate concerns to study leadership.
  • Communication & Collaboration — Work with investigators, coordinators, and monitors to ensure smooth data flow and timely completion of study deliverables.
  • Administrative Tracking — Maintain logs for data entry progress, outstanding queries, and visit completion status.
Required Qualifications
  • Education — Associate’s or Bachelor’s degree in a health-related field (biology, public health, nursing, etc.).
  • Technical Skills — Experience with EDC platforms; proficiency in Microsoft Excel and basic data management.
  • Attention to Detail — Demonstrated accuracy in data-heavy environments.
  • Clinical Research Knowledge — Understanding of GCP, ICH, and basic clinical trial workflow.
  • Communication Skills — Ability to collaborate with cross-functional teams and communicate data needs clearly.
Preferred Qualifications
  • Prior Clinical Research Experience — Experience in a research site, CRO, or academic research setting.
  • Familiarity with Medical Terminology — Ability to interpret clinical notes and lab reports.Experience with Query Resolution — Proven ability to manage sponsor/CRO queries efficiently.
Core Competencies
  • Accuracy & Thoroughness
  • Time Management
  • Confidentiality
  • Problem Solving
  • Process Improvement
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