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Contract Cra Jobs in Reston, VA (NOW HIRING)

Qiagen

Clinical Research Associate

Germantown, MD · On-site

$65K - $75K/yr

As Clinical Research Associate (CRA) you will act as the primary contact for clinical study sites ... contracts and site activation activities. * Organizing instrument set-up, operational qualification ...

TRI Challenge Convention

Central Monitor

Bethesda, MD · Remote

$18.25 - $19.50/hr

Supports one or more government or commercial contracts in multiple therapeutic areas, e.g ... as a CRA conducting on-site monitoring, or relevant skillset Knowledge of central monitoring ...

REGENXBIO

Sr Clinical Project Manager

Rockville, MD · On-site

... contract and work performed by the CRO/vendor * Oversee/responsible for the eTMF set-up ongoing ... Conducts Sponsor quality monitoring/oversight visits to sites and /or CRA performance assessment in ...

REGENXBIO

Sr Clinical Project Manager

Rockville, MD

... contract and work performed by the CRO/vendor * Oversee/responsible for the eTMF set-up ongoing ... Conducts Sponsor quality monitoring/oversight visits to sites and /or CRA performance assessment in ...

All JobsContract Cra JobsContract Cra Jobs in Reston, VA

Contract Cra information

See Reston, VA salary details

$12

$42

$72

How much do contract cra jobs pay per hour?

As of Jun 26, 2026, the average hourly pay for contract cra in Reston, VA is $42.79, according to ZipRecruiter salary data. Most workers in this role earn between $30.00 and $54.76 per hour, depending on experience, location, and employer.

What are some common challenges faced by Contract Clinical Research Associates (CRAs) and how can they effectively manage them?

Contract CRAs often juggle multiple clinical trial sites and studies, which can make prioritizing and time management especially challenging. They must adapt quickly to each sponsor's protocols and systems, often with limited onboarding. Building strong relationships with site staff and maintaining clear, consistent communication are key to overcoming these challenges. Staying organized through meticulous documentation and leveraging digital tools can help contract CRAs efficiently meet monitoring visit deadlines and regulatory requirements.

What are the key skills and qualifications needed to thrive as a Contract CRA (Clinical Research Associate), and why are they important?

To thrive as a Contract CRA, you need a solid understanding of clinical research protocols, regulatory guidelines (like GCP/ICH), and typically a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and sometimes certifications like ACRP or SOCRA are beneficial. Strong attention to detail, excellent organizational skills, and effective communication are crucial soft skills for managing multiple studies and collaborating with sites. These competencies are essential for ensuring compliance, data integrity, and the smooth execution of clinical trials.

What Are Contract CRA Jobs?

A contract clinical research associate (contract CRA) is a temporary position in which you manage clinical trials and scientific research projects. As a contractor, you work temporarily on a contract that typically lasts for the duration of the project. Clinical research associates work in the pharmaceutical industry to ensure the safety and effectiveness of medication or vaccines. You can also work on studies for biotech companies and projects that perform analysis on surgical procedures or treatments. Your duties focus on planning the trial, defining the parameters, ensuring the safety of participants, and making sure the project meets all regulations and requirements.

What are contract crafters?

Contract crafters are professionals who specialize in creating, reviewing, and negotiating contracts for individuals or organizations. They ensure that agreements are legally sound, clearly written, and protect the interests of all parties involved. Contract crafters may work in a variety of industries, including business, law, real estate, and technology. Their expertise helps minimize risk and ensure compliance with relevant laws and regulations.
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Contract Cra jobs near you
Infographic showing various Contract Cra job openings in Reston, VA as of June 2026, with employment types broken down into 61% Full Time, 23% Part Time, and 16% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $88,994 per year, or $42.8 per hour.

Clinical Research Associate

Qiagen

Germantown, MD • On-site

$65K - $75K/yr

Full-time

Medical, Vision, Life

Posted 18 days ago

Job description

Overview


At QIAGEN, we are driven by a simple but powerful vision: making improvements in life possible.

We're dedicated to revolutionizing science and healthcare for the better. From our entrepreneurial roots to our current global presence, we've grown into a force for positive change. With thousands of employees across six continents, collaboration is our greatest strength. We're always striving to identify talented individuals to join our exceptional teams.
We have played a pivotal role in shaping modern science and healthcare, and we're just getting started. If you're someone who thrives on new challenges, values diversity and wants to make a tangible difference in people's lives, then QIAGEN is the place for you.

At QIAGEN, every day is an opportunity to make a real-life impact.

Join us, grow with us, and together, let's shape the future of biological discovery.

About the Opportunity

Join our Clinical Affairs team and help advance high-quality clinical evidence for QIAGEN's innovative diagnostic solutions. You will contribute directly to studies that support the development and validation of diagnostic technologies with real-world impact on patient care.

As Clinical Research Associate (CRA) you will act as the primary contact for clinical study sites, ensuring smooth study startup, effective monitoring and highquality data collection in a regulated environment. You will be responsible for ensuring clinical research is conducted in accordance with applicable regulations and guidelines; reviewing data to confirm it meets acceptable clinical and regulatory standards; as well as protecting the rights, safety, and well-being of human subjects participating in clinical studies.

Your tasks

  • Supporting site selection, initiation, training, monitoring and closeout activities.
  • Coordinating startup processes including IEC/IRB (Ethics Committee) and regulatory submissions, contracts and site activation activities.
  • Organizing instrument set-up, operational qualification and training for testing procedures.
  • Managing study material forecasting, supply coordination and documentation according to Standard Operating Procedures.
  • Ensuring timely data collection and performing source data verification / Source Data Review, resolving data queries and supporting database verification and database lock.
  • Maintaining accurate documentation in the Trial Master File, ensuring timely upload, review and approval of study documents. Reviewing protocols, Case Report Forms and study documentation.
  • Contributing to continuous improvement initiatives by identifying opportunities to enhance clinical processes, documentation, and ways of working.

Your profile

  • Experience in Clinical Research or within the pharmaceutical, medical device or In Vitro Diagnostic (IVD) industry.
  • Understanding of clinical trial processes, IVD studies, ICHGCP and regulatory requirements.
  • Scientific or medical education; experience in molecular biology or clinical diagnostics is an advantage.
  • Experience working with external study sites and within regulated environments.
  • Familiarity with audit preparation or participation.
  • Strong communication, documentation and organizational skills with an ability to work independently while collaborating effectively with cross-functional teams.
  • Willingness to travel (up to 30%) as required.

The estimated base salary range for this position is $65,000-$75,000. Compensation will be based on the candidate's experience, skills, geographic location, and other job-related factors. In addition to base salary, we offer a total compensation package that includes a bonus plan and generous benefits.

What we offer

  • Bonus/Commission

  • Local benefits

  • Referral Program

  • Volunteer Day

  • Internal Academy (QIALearn)

  • Employee Assistance Program

  • Hybrid work (conditional to your role)

Our people are the heartbeat of everything we do. Passion drives us as we push boundaries to innovate and evolve.We inspire with our leadership and make an impact with our actions.We cultivate a collaborative, supportive environment where each individual and team can flourish. We champion accountability and encourage entrepreneurial thinking.

QIAGEN is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, or disability.

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