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What is a CRO cra?

CRO CRAs, or Clinical Research Associates working for Contract Research Organizations (CROs), are professionals who monitor clinical trials to ensure compliance with regulatory requirements and study protocols. They act as the link between the sponsor of the clinical trial and the sites conducting the research. Their responsibilities include site selection, study initiation, monitoring visits, data verification, and ensuring patient safety. CRO CRAs often work on multiple studies for different sponsors, providing flexibility and exposure to a variety of therapeutic areas.

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Cro Cra is typically considered an entry-level position that may require basic skills related to the specific industry or role. It often involves on-the-job training and does not usually require extensive prior experience or advanced certifications.

Is it hard to get a clinical research associate job?

Securing a clinical research associate (CRA) position can be competitive, often requiring a relevant degree in life sciences or healthcare, along with experience in clinical trials. Strong knowledge of Good Clinical Practice (GCP) guidelines and certification can improve job prospects, but the level of difficulty varies based on location and individual qualifications.

What are the key skills and qualifications needed to thrive as a CRO (Chief Revenue Officer), and why are they important?

To thrive as a Chief Revenue Officer (CRO), you need a strong background in sales, marketing, business development, and financial management, often supported by a relevant degree and significant leadership experience. Familiarity with CRM platforms (like Salesforce), analytics tools, and revenue management systems is typically required. Outstanding strategic thinking, communication, and cross-functional leadership skills set exceptional CROs apart. These competencies are essential for driving company growth, aligning teams, and optimizing revenue streams in a competitive market.

What are some of the most common challenges faced by a CRO (Conversion Rate Optimization) manager, and how can they be addressed?

A CRO Manager often faces challenges such as aligning optimization strategies with broader business goals, managing stakeholder expectations, and balancing short-term wins with long-term improvements. It's essential to establish clear communication with marketing, product, and development teams to ensure experiments are prioritized effectively. Data-driven decision making, consistent A/B testing, and staying updated on user behavior trends can help overcome these challenges and drive meaningful results.
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Clinical Research Associate (CRA) II

CVRx, Inc.

Brooklyn Park, MN • On-site, Remote

Full-time

Medical, Dental, Life, Retirement, PTO

Re-posted 8 days ago

Job description

Why work for CVRx?

CVRx pioneers' unique therapies that harness and harmonize the body's natural systems, benefiting society and making CVRx a universal role model in healthcare. We value our commitments to others and continue to overcome challenges through determination, collaboration and purpose. If our culture and values speak to you, and if you have a passion for cutting-edge medical technologies, join our team and our mission to help others live better lives.

This position is remote. Our ideal candidate will reside near our headquarters in Brooklyn Park, MN for occasional on-site visits.  

The Role
The Clinical Research Associate (CRA) II performs the day-to-day operations associated with the execution of clinical trials and is responsible for the direct contact with assigned clinical investigative sites. The CRA II will coordinate site activities from site start-up to site closure as needed. The CRA II will ensure the overall quality of the clinical sites by reviewing study data and managing site adherence to the protocol, Good Clinical Practice (GCP), and all applicable regulations. The CRA II will work closely with the other CRAs on the clinical team and project managers to ensure the sites maintain compliance.  
KEY DUTIES AND RESPONSIBILITIES
  • Proactively maintains timelines for assigned or requested deliverables.
  • Develops and maintains successful working relationships with study sites and CVRx field staff
  • Assists in preparation of study materials and training of investigators and research site staff
  • Becomes proficient with all study databases, systems and company quality management system 
  • Reviews and verifies clinical data/information and oversees data correction to match source   
  • Acts a site manager and monitor to assigned sites as applicable per study requirements
  • Processes payments to sites, vendors, and consultants. Supports the Clinical Project Manager with study finance activities and tracking
  • Supports Clinical Centers in the execution of site Institutional Review Board (IRB) or ethics committee (EC) submissions
  • Responsible for the collection, tracking, and maintaining required study and regulatory documents from clinical centers through all phases of assigned projects
  • Prepares study materials and trains investigators and site staff
  • Responsible for shipment of study-related materials as applicable
  • Coordinates and conducts monitoring (as directed by the monitoring plan) at participating centers to ensure compliance with protocol, regulations, and the timely receipt of accurate data / other required study documents
  • Reviews and verifies clinical data/information and oversees data correction to match source
  • Reviews monitoring reports
  • Manages device accountability at site (if applicable)
  • Provides input to study budgets and project plan
  • Contributes to maintaining oversight of activities conducted by Contract Research Organizations (CRO's) or other contractors on behalf of CVRx (if applicable)
  • Assists in training or mentorship of new Clinical Research Associates
  • Completes special projects and performs job-related duties as assigned
 
REQUIRED EDUCATION, TRAINING AND JOB-RELATED EXPERIENCE
  • Bachelor's degree or advanced degree in science or a related field, or equivalent work experience
  • 2-4 years experience directly supporting clinical research or similar experience in a medical/scientific area
  • Knowledge of medical terminology
  • Experience with GCP's and regulatory compliance guidelines for clinical trials
  • High attention to detail and accuracy
  • Ability to manage multiple tasks and operate independently
  • Operates in an efficient and expedient manner
  • High ethical standards and integrity
  • Experience working on cross-functional teams
  • Comfortable in a small company and thrives in a high-growth environment
  • Advanced written and oral communications skills
  • Good problem-solving skills
  • Adaptable and embraces change
  • Creative and resourceful
  • Team player with high performance standards
  • Entrepreneurial approach
PREFERRED EDUCATION, TRAINING AND JOB-RELATED EXPERIENCE

  • Advanced degree in a related field

 
 
WORKING CONDITIONS AND REQUIRED PHYSICAL EFFORT
  • Normal office conditions and a reliable internet connection when working in a home office
  • Must be able to sit/stand/walk 8 or more hours per day
  • Position requires up to 40% travel
  • May be required to be fully vaccinated against the COVID-19 virus and other diseases.
 

CVRx is unable to provide employment visa sponsorship for this position. Candidates must be legally authorized to work in the United States without current or future sponsorship

What we offer:

CVRx is proud to offer competitive salaries and benefits plans.

We offer a culture of teamwork, collaboration, and positivity, where challenging the status quo is welcomed, continuous learning is valued, and each of us has an opportunity to make a significant impact in an exciting, purpose-driven startup environment while also having fun.

Salary range for U.S locations (USD): 85,000 - 105,000 per year.

The pay range is applicable across the U.S., complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and specific location. 

We also offer a competitive and rewarding benefits package, details listed below:

  • Competitive Health & Dental Insurance options with generous Company contributions 
  • Company contributions to an HSA with a high deductible insurance plan selection
  • 401(k) with a company match
  • Employee stock purchase plan (ESPP) & stock option and RSU grants
  • 12 company-paid holidays per year in addition to a generous Flex PTO plan
  • Generous paid time off for new parents
  • Company-paid life insurance & disability options
  • Unlimited growth opportunities in a growing company
  • Endless training & learning opportunities
  • Flexible Schedule

EEO STATEMENT

CVRx, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.   

This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.  

If you're an independent, self-motivated individual with excellent interpersonal skills, a desire to do great things and have a background in medical devices, healthcare or a related field, we want to hear from you!   

If you need assistance or an accommodation due to a disability, you may contact us at [email protected] 

CVRx Privacy Policy 
CVRx SMS Terms of Service 

This requisition will be open until filled.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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