Join Our Team

Aperio is a different kind of CRO.

At Aperio, we hire the brightest minds and best talent every day to work on our sponsors’ clinical trial programs. But we don’t stop there. We pride ourselves on being a company where employees can be heard and make a difference. Our employees are visionaries, innovators, critical thinkers and disruptors. We invite them to be creative, to think outside-the-box and to have a voice. They offer us fresh perspectives, ask the hard questions, challenge our blind spots and make us better every day.

But this isn’t just a job or a company – Aperio is a family. We care about one another. We are collaborative, flexible and value trust and transparency. We encourage personal growth and development, practice recognition and hold one another accountable to maintain a healthy work-life balance.

Ready to work with some of the industry’s greatest talent? Looking for a work-home where you can be challenged, heard and enjoy a sense of belonging? Consider applying for one of our current job openings today.

What you’ll be doing:

  • You will manage a data management project, what does that include:
    • Own your own studies and project deliverables
    • Identify roadblocks, overcome hurdles and provide solutions
    • Review budgets
  • You will manage clinical data and query review
  • Create the Data Review Plan
  • Issue queries and review query responses
  • Reconciliation (LAB, SAE, ECG, and other vendors)
  • You will oversee system development and modifications:
    • Draft the CRF design, edit check specification and DM listings
    • Manage all database build and modifications
  • You will create and maintain documentation for assigned projects
    • Data Management Plan, CRF Completion guidelines, Data Entry guidelines, Edit specifications, Reconciliation guidelines and Report specifications
    • Database release documentation
    • Project Specific SOPs/WPs
  • Performs other duties – what do you want to learn?

What we are looking for in a candidate:

  • BA/BS degree required with 10 years of experience in clinical research (8 years in data management); OR
  • 12 years of experience in clinical research (10 years in data management) may be accepted in lieu of a degree
  • Experience with Microsoft Office suite and strong working knowledge of electronic data capture systems (Medidata Rave preferred)
  • Knowledgeable in Clinical Research, ICH GCP and medical terminology
  • Ability to travel occasionally

 

Aperio Clinical Outcomes 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.

 


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What you’ll be doing:

  • You will have the opportunity manage all necessary programming tasks to implement an EDC system
  • Let your leadership skills shine by providing coaching and mentoring to other programming staff as needed
  • Apply your expert knowledge to contribute to process improvement
  • Create and manage departmental study documentation
  • Expand your knowledge and expand your skillset within the CRO industry

What we are looking for in a candidate:

  • Strong working history in EDC programming within the clinical trials industry
  • Practical experience programming in Medidata Rave specifically
  • Degree or certificate preferred in Computer Science, Information Systems Management, or related field
  • Proficient experience with various computer applications (Windows, Excel, Word, Outlook, etc.)
  • Ability to travel occasionally

 

Aperio Clinical Outcomes 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.

 


APPLY

We’re always expanding our network of qualified clinical research professionals.

Offering both full and part-time positions, we match clinical research professionals with job opportunities, whether you are an independent contractor or prefer employee status.

We are always accepting resumes for the following roles: 

  • Senior CRA (Clinical Research Associate)
  • Senior Project Manager (PM)
  • CTM (Clinical Trial Manager)
  • Clinical Support Specialist
  • Proposal Analyst
  • Project Financial Analyst (PFA)
  • Lead Clinical Data Manager
  • Clinical Data Specialist
  • EDC Programmer
  • SAS / Analytics Programmer
  • Medical Writer
  • Medical Monitor

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