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Cro Entry Jobs (NOW HIRING)

CPI Security

Chief Revenue Officer

Charlotte, NC · On-site

... entry, and M&A execution. The CRO will oversee high-performing sales and business development teams while building scalable processes, partnerships, and programs to support rapid growth and long-term ...

CPI Security

Chief Revenue Officer

Charlotte, NC · On-site

... entry, and M&A execution. The CRO will oversee high-performing sales and business development teams while building scalable processes, partnerships, and programs to support rapid growth and long-term ...

McLaren

Coordinator Clinical Research

Flint, MI · On-site

$23.50 - $31.25/hr

... entry to clinical trials, and assisting the other staff in determining eligibility of potential ... CRO in a timely manner as dictated by the study protocol. 5. Coordinates tests and procedures as ...

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Cro Entry information

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How much do cro entry jobs pay per hour?

As of Jun 7, 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 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 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.
More about Cro Entry jobs
What cities are hiring for Cro Entry jobs? Cities with the most Cro Entry job openings:
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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 May 2026, with employment types broken down into 2% Locum Tenens, and 98% Full Time. Highlights an 73% Physical, 4% Hybrid, and 23% Remote job distribution, with an average salary of $37,275 per year, or $17.9 per hour.
Clinical Trial Manager - Contractor

Clinical Trial Manager - Contractor

Arcus Biosciences

Brisbane, CA • On-site, Remote

Contractor

Posted 11 days ago

Job description

Description
Summary
The Clinical Trial Manager (CTM) will provide clinical study support to the Clinical Program Manager/Study Management Team Lead (SMTL) for one or more clinical studies, ensuring efficient delivery of clinical trials in a matrix environment. Key accountabilities include assuring successful conduct of clinical studies consistent with applicable regulations, guidelines and procedures, as well as supporting clinical project timelines, contracts, budgets, vendor management, invoicing, accruals, oversight monitoring visits, meeting milestones and deliverables, and internal/external communications. This position is remote or in-house, depending on prior experience. This position will report to a Clinical Operations Manager. Bay Area staff will operate in a hybrid or office based model aligned with Arcus expectations.
Responsibilities
  • Day-to-day management of assigned operational aspects of low to medium complex clinical trials, including but not limited to vendor/ laboratory management, oversight of clinical sites, etc.
  • Obtains and reviews all required essential documents necessary for study/site initiation
  • Maintains/files accurate and timely sponsor/site correspondence and communication. Prepares and presents project progress reports
  • Manages and tracks patient enrollment, site performance and monitoring metrics
  • Performs tasks in accordance with ICH GCP, regulations, the protocol, and company SOPs/Policies
  • Supports the development and review of clinical study plans, presentations or study-related documents
  • Support in the development and design of CRFs, including participating in the EDC and IXRS specification process and UAT on related systems
  • Assists with set-up of central labs and study vendors as required, including liaising with Clinical Program Manager and CRO to ensure site training and timely initiation of clinical study sites
  • Performs in-house review of clinical data listings for completeness and accuracy and escalate issues to the Clinical Program Manager, as needed
  • Works closely with data management lead to perform data cleaning activities with cross-functional team
  • May lead and coordinate protocol deviation review and documentation
  • Manage clinical monitoring activities and the overall site management ensuring compliance with Good Clinical Practices (GCP) and applicable regulations and tracking of site performance metrics
  • May perform accompanied site visits with CRO Site Monitors to ensure correct study procedures according to SOPs and protocol procedures, review of routine regulatory documents/files in compliance with protocol, regulatory requirements, site and CRO SOPs, and study plans, as required
  • Reviews monitoring trip reports and track resolution of all action items
  • Participates in the selection, training, and evaluation of study personnel (vendor, CRO, internal)
  • Assists with providing oversight of CROs and vendors
  • 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 team meetings, investigator meetings, and other trial specific meetings, as requested
  • Contributes to development and review of clinical trial documents such as clinical protocol, informed consent form(s), patient facing materials, etc.
  • Provides support in the development and management of vendor scope of work (SOW) per contract, quality, budget, and detailed timelines including investigator and vendor payments, as applicable
  • Recommend and implement innovative ideas to increase efficiency and quality of program management activities
  • Contributes to process and departmental and cross-functional improvement activities

Qualifications
  • Bachelor's degree, preferably in a scientific field
  • 5+ years of related industry experience in the pharmaceutical industry or equivalent, plus 2+ years of trial management experience, preferably in oncology
  • Demonstrates core understanding of clinical trial related terminology and activities
  • Thorough understanding of ICH GCP guidelines and Code of Federation Regulations
  • Understanding of clinical trial processes from study start-up through study closure
  • Ability to establish priorities, sense of urgency and collaborate (interpersonal, relationship management) with the study team, cross functional team members and external partners/vendors
  • Excellent planning and organization skills
  • Self-motivated, assertive, and able to function independently and as part of a team
  • Strong interpersonal and negotiation skills as well as strong verbal and written communication (including presentation of materials to internal teams and external partners)
  • Excellent IT Microsoft skills and experience using clinical trial management web-based systems (i.e. EDC, IRT, CTMS, eTMF, etc.)
  • Ability and willingness to travel 10-20% (domestic and international)
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