ZipRecruiter

Log In

1

Cro Entry Jobs in Indiana (NOW HIRING)

IQVIA

CRA 1, IQVIA Biotech

Indianapolis, IN · On-site

$71K - $145K/yr

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of ... entry and query resolution, and ensure maintenance of both the Trial Master File (TMF) and the ...

IQVIA

CRA 1, IQVIA Biotech

Indianapolis, IN · On-site

$71K - $145K/yr

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of ... entry and query resolution, and ensure maintenance of both the Trial Master File (TMF) and the ...

All JobsCro Entry JobsCro Entry Jobs in Indiana

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 Indiana? For Cro Entry jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Cro Entry jobs in Indiana look for? The top searched job categories for Cro Entry jobs in Indiana are:
What cities in Indiana are hiring for Cro Entry jobs? Cities in Indiana with the most Cro Entry job openings:
Cro Entry jobs near you
Infographic showing various Cro Entry job openings in Indiana as of July 2026, with employment types broken down into 92% Full Time, and 8% Part Time. Highlights an 93% In-person, 2% Hybrid, and 5% Remote job distribution.

Clinical Research Coordinator II - New Albany, IN

Iterative Health

New Albany, IN

$22.50 - $29.75/hr

Other

Posted 18 days ago

Job description

Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 80+ global clinical research sites accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies. Our focus is on driving the success and growth of our partner sites by empowering them with tech-enabled services. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.

We are seeking a full-time, experienced Clinical Research Coordinator - Level II (CRC II). The CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.  

Responsibilities:

  • Administratively and clinically manage industry-sponsored clinical trials including problem solving, communication and protocol management. Manage a full schedule of complex study visits and corresponding tasks with minimal direction. 
  • Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies, with accountability for achieving enrollment goals
  • Schedule all patient research visits and procedures consistent with protocol requirements
  • Conduct patient visits as outlined within each study protocol
  • Dispense study medication, collect vital signs and perform ECGs
  • Perform blood draws, process and ship specimens per study protocol and IATA regulations
  • Ensure relevant study and subject specific information is entered into the CTMS system on a regular basis; complete and maintain documentation study files including, but not limited to, consent forms, source documentation, progress notes if applicable, case report forms, and investigational accountability forms. Maintain high quality data entry within established timelines
  • Act as point of contact for study participants
  • Adhere to Research SOPs, Good Clinical Practices, and the study protocols
  • Maintain ongoing communication with the CRO, sponsor, research participants, Site  Manager, central Iterative Health team, and PI throughout the study. Resolve routine sponsor and CRO issues independently
  • Ensure all safety data is reviewed by the PI in a timely manner
  • Maintain inventory of study equipment and supplies onsite at all times
  • Contribute to status updates to management; contribute and implement ideas to improve site performance 
  • Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol. Meet requirements for data query resolution times and quality. 
  • Schedule and prepare for monitor visits
  • Assists Study Team in protection of the rights and welfare of all human research participants involved in research in accordance with Federal regulations
  • Cooperates with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance 
  • Complete and maintain case report forms per FDA guidelines, and review them against the patient's medical record for completeness and accuracy

Iterative Health Expectations

All employees are expected to:  

  • Perform quality work within deadlines with or without direct supervision
  • Interact professionally with other employees, customers and suppliers
  • Work effectively as a team contributor on all assignments
  • Work independently while understanding the necessity for communicating and  coordinating work efforts with other employees and organizations

Qualifications

  • Medical Assistant, LPN, Associates or Bachelor's degree in a clinical or scientific-related discipline preferred
  • Minimum 3 years of clinical research experience
  • IBD experience is a must
  • Ability to own issues and problem solve independently 
  • Experience in phlebotomy preferred
  • Strong written and verbal communication skils
  • Ability to read, interpret, and apply clinic policies and research protocols
  • Ability to use standard office software
  • Must be able to lift up to 25 pounds

At Iterative Health, we're actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.

Apply