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.
What you’ll be doing:
- Create and maintain programs that generate analytical datasets, listings, and reports
- Create and maintain documentation for testing and versioning of programs
- Collaborate with internal and external stakeholders regarding reporting requirements and specifications and provide updates on the status of analytics projects
- You will have the opportunity to collaborate with as well as mentor and train programming colleagues
- Support the department with standardizing programming procedures
- Support the reporting infrastructure administration including permissioning, performance testing, and scheduling programs
- Performs other duties – where can your talents shine?
What we are looking for in a candidate:
- Bachelor’s degree in Mathematics, Statistics, Computer Science, or related field
- A minimum of 3 years of analytics programming experience in bioinformatics, healthcare, or clinical research
- Proficiency in analytical coding software
- Strong SAS (Base SAS, SAS/Macro, and SAS/Graph) skills
- Experience with Electronic Data Capture (EDC) data exports
- Proficiency in merging multiple datasets
- Strong critical thinking, creativity, and problem solving skills
- Strong communication and collaboration skills
- Strong time management, flexibility, and multi-tasking skills
- Strong analytical and risk assessment skills
- Good technical writing skills
- Good knowledge in automation and file sharing software
- Strong ability to learn new programming languages, technologies and tools
- Excellent knowledge of FDA regulations, ICH guidelines, and GCPs – and their application to clinical trials
- 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.
What you’ll be doing:
- You will have the opportunity to lead and manage all necessary EDC programming activities from implementation though ongoing maintenance (including database migrations, and eventually study closure
- Let your leadership skills shine by providing coaching and mentoring to other programming staff
- Apply your expert knowledge to contribute to process improvement
- You will be relied upon to identify and escalate issue or inconsistencies
- Create and manage departmental study documentation
- You will also have the opportunity to provide programming support for non-EDC tasks to data management staff or other Aperio staff e.g., custom reports, and Excel macro development
- What drives you, where else can your contributions make an impact?
What we are looking for in a candidate:
- Bachelor’s degree in computer science or related field
- Strong working history programming in Medidata Rave in the clinical trials industry
- Experience in C# programming, specifically custom function programming in Medidata Rave
- Proficiency in related clinical trial technology integrations
- Good critical thinking, creativity, and problem-solving skills
- Strong productivity, prioritization, and planning skills
- Strong communication and interpersonal skills (verbal and written), with the ability to establish rapport and build relationships
- Strong time-management, flexibility, and multitasking ability
- Strong attention to detail and organizational skills
- Strong analytical and risk assessment ability
- Good understanding of study budgets
- 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.
What you’ll be doing:
- Collaborate with internal and external stakeholders on the design and successful implementation of a customized data reporting tool for multiple clinical trials.
- Apply your curiosity and knowledge to utilize the data reporting tool and identify signals and trends of assigned data analytics projects; support study teams with actionable follow ups to mitigate issues.
- Participate in specification, testing, and enhancements of the data reporting tool to support the study specific needs our clients.
- You will have the opportunity and responsibility of preparing training materials and implementing customized workshops to support data tool users.
- Maintain relationships with users and provide high quality, consultative support throughout the study.
- Contribute your knowledge and expertise to participate in various business development demonstrations, marketing case studies highlighting client success and industry focused presentations.
- Collaborate with team members on the development and implementation of operational documents and procedures.
- Performs other duties – where can your talents shine?
What we are looking for in a candidate:
- Bachelor’s degree in health sciences, analytics, or related area
- 5 years of clinical research experiences (some clin ops preferred)
- Strong knowledge of data management and EDC programming
- Strong proficiency with understanding clinical data structures and relational databases
- Strong knowledge of relational databases and unique data collection
- Strong knowledge on data integration, analysis of data, and presentation of results
- Strong critical thinking, creativity, and problem-solving skills
- Strong time management, flexibility, and multi-tasking skills
- Strong attention to detail and organizational skills
- Strong analytical and risk assessment skills
- Strong technical writing skills
- Strong ability to provide constructive feedback and deliver difficult conversations, with intent to obtain positive results
- Strong productivity, prioritization, and planning skills
- Strong communication and interpersonal skills (verbal and written), with the ability to establish rapport and
- Strong collaboration skills with cross-functional teams
- Excellent knowledge of FDA regulations, ICH guidelines, and GCPs – and their application to clinical trials
- 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.
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