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Cro Entry Jobs in California (NOW HIRING)

Oruka Therapeutics

Accounting Manager

Menlo Park, CA · Hybrid

$146K - $161K/yr

... journal entry preparation, account reconciliations, and flux analysis. * Hands-on experience with clinical trial or R&D accruals, including CRO and vendor expense management. * Exceptional ...

Exelixis

Clinical Trials Manager (Oncology)

Alameda, CA · On-site

... CRO oversight on activities related to site start-up and maintenance, including reviewing trip ... Experience/The Ideal for Successful Entry into Job: • Typically requires a minimum of 7 years of ...

Exelixis

Clinical Trials Manager (Oncology)

Alameda, CA · On-site

Provides CRO oversight on activities related to site start-up and maintenance, including reviewing ... Experience/The Ideal for Successful Entry into Job: * Typically requires a minimum of 7 years of ...

Exelixis

Vice President, Biostatistics

Alameda, CA · On-site

Provides executive leadership for sponsor/CRO activities, relationships and escalation resolution ... Experience/The Ideal for Successful Entry into Job: * PhD in related field strongly preferred * In ...

Exelixis

Vice President, Biostatistics

Alameda, CA · On-site

Provides executive leadership for sponsor/CRO activities, relationships and escalation resolution ... Experience/The Ideal for Successful Entry into Job: * PhD in related field strongly preferred * In ...

Exelixis

Vice President, Biostatistics

Alameda, CA · On-site

Provides executive leadership for sponsor/CRO activities, relationships and escalation resolution ... Experience/The Ideal for Successful Entry into Job: * PhD in related field strongly preferred * In ...

Ionis

Clinical Trial Management Associate

Carlsbad, CA · On-site +1

$34.50 - $47.25/hr

Ensures timely study entry and updates to ClinicalTrials.gov * Assists with design and preparation ... Participates in co-monitoring activities and oversight of CRO or contract CRAs for pre-study ...

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Showing results 1-20

All JobsCro Entry JobsCro Entry Jobs in California

Cro Entry information

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.
What are popular job titles related to Cro Entry jobs in California? For Cro Entry jobs in California, the most frequently searched job titles are:
What job categories do people searching Cro Entry jobs in California look for? The top searched job categories for Cro Entry jobs in California are:
What cities in California are hiring for Cro Entry jobs? Cities in California with the most Cro Entry job openings:
Cro Entry jobs near you
Clinical Trial Assistant

Clinical Trial Assistant

SAGIMET BIOSCIENCES INC.

Foster City, CA • On-site

$75K - $90K/yr

Other

Posted 12 days ago

Job description

Description

The Clinical Trial Assistant (CTA) provides operational and administrative support to the Clinical Operations team in the execution of Sagimet's clinical trials. This role requires a highly organized, detail-oriented individual who can manage multiple priorities and contribute across a broad range of clinical and regulatory activities. The CTA will play a hands-on role in trial start-up, maintenance, and close-out activities, partnering closely with Clinical Trial Managers (CTMs),, vendors, and cross-functional internal stakeholders. The CTA will report to the Senior Vice President, Clinical Operations.


Essential Responsibilities:

  • Maintain,  organize and QC Trial Master Files (TMF/eTMF) to ensure inspection readiness at all times
  • Assist with study start-up activities, including collection and tracking of regulatory documents (e.g., 1572s, CVs, licenses, IRB/EC approvals)
  • Support site activation, maintenance, and close-out processes
  • Track and manage clinical trial documentation, ensuring accuracy, completeness, and timeliness
  • Assist with creation, review, and formatting of study-related documents (protocols, manuals, study plans, etc.)
  • Prepare or oversee CRO with clinical trial materials including investigator site binders, study tools, and training materials
  • Assist CRO and internal team with oversight of sample tracking vendor and dashboard. 
  • Track operational deliverables, timelines, and key milestones
  • Assist in organizing investigator meetings, vendor meetings, and internal study team meetings
  • Draft meeting agendas, capture meeting minutes, and follow up on action items
  • Maintain study tracking tools and spreadsheets (e.g., site lists, enrollment trackers, document trackers)
  • Support review of data entry and reconciliation activities across systems (e.g., CTMS, eTMF, EDC where applicable)
  • Assist in the preparation of status reports and dashboards for internal stakeholders
  • Ensure compliance with GCP, SOPs, and applicable regulatory requirements
  • Support audit and inspection readiness activities, including documentation preparation and QC
  • Assist in tracking and filing safety reports and regulatory submissions
  • Provide administrative support to the Clinical Operations team as needed
  • Manage document version control and filing systems
  • Support cross-functional collaboration with Regulatory, Quality, and Clinical Development
  • Other duties as assigned


Requirements

Education and Experience Requirements:


  • Bachelor's degree in life sciences, healthcare, or related field preferred 
  • 2-4 years of experience in clinical research, clinical operations, or a related field 
  • Experience in a biotech, pharma, or CRO environment preferred; startup experience a plus
  • Strong organizational skills with exceptional attention to detail 
  • Ability to manage multiple tasks and prioritize effectively in a fast-paced environment 
  • Excellent written and verbal communication skills 
  • Proficiency with Microsoft Office (Word, Excel, PowerPoint); familiarity with CTMS/eTMF systems preferred 
  • Understanding of ICH-GCP guidelines and clinical trial processes

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