ZipRecruiter

Log In

1

Cro Entry Jobs (NOW HIRING)

PSI CRO

Clinical Study Coordinator

Tulsa, OK · 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 ...

PSI CRO

Clinical Study Coordinator

Cleveland, TN

... 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

Clinical Study Coordinator

Tulsa, OK · 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 ...

PSI CRO

Clinical Study Coordinator

Cleveland, TN · 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 ...

PSI CRO

Clinical Study Coordinator

Tulsa, OK

... 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 ...

PSI CRO

MO

... 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

... 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

... 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

$16.50 - $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 ...

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 ...

VALENCIA HOTEL 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 ...

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 ...

next page

Showing results 1-20

All JobsCro Entry Jobs

Cro Entry information

See salary details

$12

$17

$22

How much do cro entry jobs pay per hour?

As of Jul 11, 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.

How do I get into a CRO?

To enter a Conversion Rate Optimization (CRO) role, develop skills in data analysis, user experience, and A/B testing, often using tools like Google Optimize or Optimizely. Gaining experience through internships, certifications, or working on digital marketing projects can also improve your chances of entering the field.

What are CRO Entry jobs?

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 jobs pay 4000 a week without a degree?

Jobs that can pay $4,000 a week without a degree often include skilled trades such as commercial truck driving, construction management, or certain sales roles like real estate or high-ticket sales. These positions typically require specialized skills, certifications, or experience, and may involve long hours or physically demanding work.

What jobs pay $500,000 a year in the US?

High-paying jobs that can reach or exceed $500,000 annually include roles such as senior corporate executives (CEOs, CFOs), successful entrepreneurs, top-tier investment bankers, and certain specialized medical professionals like neurosurgeons. These positions often require extensive experience, advanced skills, and in some cases, ownership or leadership of large organizations or practices.

What are some common challenges faced by professionals in a CRO (Conversion Rate Optimization) Entry role, 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.

What are the key skills and qualifications needed to thrive as a CRO (Conversion Rate Optimization) Entry-level Specialist, and why are they important?

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.

Is it hard to get a CRA job?

Getting a CRA (Clinical Research Associate) job can be competitive, often requiring relevant education such as a degree in life sciences or healthcare, along with experience in clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and familiarity with clinical trial management systems can improve chances of employment. Certification, like the CCRA, may also enhance prospects but is not always mandatory.
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 job categories do people searching Cro Entry jobs look for? The top searched job categories for Cro Entry jobs are:
Cro Entry jobs near you
Infographic showing various Cro Entry job openings in the United States as of July 2026, with employment types broken down into 91% Full Time, and 9% Part Time. Highlights an 92% In-person, 2% Hybrid, and 6% Remote job distribution, with an average salary of $37,275 per year, or $17.9 per hour.

Clinical Study Coordinator

PSI CRO

Tulsa, OK • On-site

Full-time

Posted 24 days ago

Job description

Company Description
Milestone One is a Site Enabling Services organization with global headquarters in Zug, Switzerland. We understand what clinical study sites need and our overall mission is to support sites in stronger study delivery.
Job Description
The Site/Study Coordinator supports a medical institution in clinical trial-related activities. Protocol-specific tasks will be determined by the Principal Investigator, considering all local and federal laws and regulations and upon review of competencies observed and documented by Milestone One. Tasks may include activities associated with the assessment of the feasibility of new/potential clinical studies, conducting research-related visits as outlined in the respective protocol, assisting the site with logistics of scheduling research visits and testing per the schedule of events in the protocol, collaboration with ancillary departments involved in the research visit to assist in a smooth patient flow at research visits., general study conduct tasks, assistance with data 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 addition, mentoring staff and administrative tasks as assigned by the Milestone One Manager.
In this job you will:
  • Acts as a constant line of communication between Milestone One, the Sponsor or CRO, and the medical institution.
  • Facilitates the evaluation of proposed studies and ensures responses to feasibility questions are provided in due time.
  • Actively participates in patient recruitment/identification and evaluation for study inclusion by confirming eligibility according to the Inclusion and exclusion criteria.
  • Assists with plan development for new recruitment / retention tools, source documentation and other site tools to enhance quality and time management of research staff.
  • Assists the local research team in obtaining informed consent before study entry or any study-related procedures or tests being performed.
  • Assist with obtaining the required assessments at each visit per the protocol and notify the investigator of any critical values that need immediate attention or would prohibit or delay study treatment.
  • Assist with obtaining local and central laboratory testing, processing, and shipping per site SOP and study-specific lab manual.
  • Assist in scheduling and preparation for all types of sponsors or CRO representative visits at the medical institution.
  • Track patient recruitment and enrollment and actively supports the medical site team to ensure enrollment targets are met at the site level. Provides regular updates to the staff and investigators regarding study amendments.
  • Ensure accurate and timely data entry into study-specific EDC systems, resolves data queries, and assists in reporting and following up on adverse events and protocol deviations according to guidelines and investigator instructions.
  • Support proper handling, accountability, and reconciliation of all investigational products and clinical supplies. If applicable, always maintain the study blinding. Protocol and sponsor/CRO guidance will be followed if a study participant requires unblinding.
  • Assist site staff with maintaining appropriate temperature monitoring for study products and supplies.
  • Support the contract and budget negotiations and oversees Investigator/Site Payments.
  • Ensure that all staff participating in a clinical trial complete all necessary study-specific and general training before their involvement in the trial. Retraining will be completed for changes to the protocol before site implementation.
  • Be responsible for ensuring the investigator reviews and signs study documents appropriately and within a reasonable period. Guidance should be provided to educate the site research team on requirements for conducting clinical trials, date format, etc.
  • Actively participate in maintaining study documents at the medical institution in preparation for on-site study visits/audits or regulatory agency inspections.
  • Assist with preparing and submitting regulatory documents and correspondence to regulatory authorities and institutional review boards (IRBs).
  • May be involved in the on-site training of additional staff as part of the SEO or other education programs.
  • Assist with identifying areas that need improvement for specific sites and assists with developing tools to assist with improvements.
  • Maintain all licensure and certifications applicable to the role of SEO site/Study coordinator II.
  • SEO SC is responsible for only performing assigned tasks within their training and licensure if applicable. SEO SC should immediately consult the assigned Milestone One manager for tasks that do not fall within their scope.

Qualifications
Education
Relevant education and at least two years of experience coordinating clinical research studies involving human subjects OR, if allowed by local regulations, on-the-job training with at least two years of experience coordinating clinical research studies involving human subjects.
Certifications
  • Current Good Clinical Practice (GCP)
  • International Air Transport Association (IATA)
  • Current Basic Cardiopulmonary Resuscitation (CPR)
  • Phlebotomy certification unless part of active professional licensure (RN or LPN)
  • Preferred Certification in Clinical Research by ACRP or SOCRA or another approved Clinical Research Organization. May be obtained within (1) year of employment or status change if not currently certified.

Additional Information
Location: Tulsa, OK
If you feel it is time to make your skills and knowledge visible within a developing company with true focus on its people, then Milestone One is the right choice for you!

Apply