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Sr. Clinical Research Associate

Avania

Remote · USResearchup to $140K/yrSeen todaySeen in employer's feed today

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At a glance

Compensation
up to $140K/yr
Location
Remote · US
Role Type
Research
Work Authorization
Not specified

Olive lists jobs from US employers, including remote roles you can work from the United States.

Job overview

Avania is hiring Senior Clinical Research Associates based in Pennsylvania, Maryland, and/or New York to oversee clinical trials and protect participant rights while ensuring accurate, verifiable data and protocol compliance. The role includes site monitoring, regulatory and document review, trial start-up support, and possible Clinical Lead responsibilities. Candidates need medical device experience and at least four years of relevant CRA work; travel may reach 75%.

Skills & qualifications

RequiredNice to have

Skills

Clinical Trial MonitoringMedical Device ExperienceTracker ManagementClinical Trial Start-UpSpreadsheet SkillsMedical KnowledgeGCP-ICH-E6FDA RegulationsISO 14155ISO 13485ISO 9001Medical Device RegulationsClinical Trial RegulationsCommunicationPresentation SkillsRapport BuildingPlanning and PreparationInformation GatheringTask PrioritizationProactive AttitudeRespiratoryCardiovascular

Qualifications

Bachelor's in Related Discipline or Equivalent Experience4+ Years CRA ExperienceClinical Lead ExperienceUp to 75% Travel

Benefits

Tuition Assistance

Full job description

Avania is hiring 2 x Senior Clinical Research Associate (Sr CRA) based PA, MD and New York

Salary Range up to $140,000 + Annual Performance related bonus + Benefits

Avania’s ClinOps Team establishes, maintains and supports clinical trials; as a key member of the team, our Sr CRA performs clinical trial oversight for the trials, verifying that the rights and well-being of human subjects are protected, and that reported trial data are accurate, complete, and verifiable (from source documents).

Partnering closely with our Trial sites, Avania's Sr CRA ensures that the conduct of the trial follows approved protocols/amendment(s), with ISO14155 or ICH-GCP, and with applicable regulatory requirements.

Our Senior CRA role includes the following key activities -

  • Interact with and guide study investigators and study coordinators in conducting clinical trials in accordance with study protocols. Member of a site Start-up Team for assigned projects.

  • Monitor site’s completion of action items between visits and help prepare for audits and inspections; conduct and write accurate visit reports in accordance with SOPs and GCP (SQV, SIV, IMV, COV)

  • Ensure data entered on the CRFs is timely, accurate and verified. Collaborate with analytical services to obtain clean database, resolve queries and conduct or participate in data reviews (both internally and with sponsor), identifying and communicating trends or erroneous data.

  • Participate in internal TMF reviews, as needed.

  • Develop and maintain trackers, such as visit reports trackers, site trackers, recruitment and enrollment trackers.

  • Review and write informed consent forms. Review of protocols, investigator brochures on compliance with applicable regulations and CRFs in development. Prepare clinical trial agreements and present to site and study sponsor.

  • Review regulatory compliance for study documents and protocols.

  • May act as a Clinical Lead, overseeing clinical trial activities at investigational sites (will require travel to investigational sites).

Candidates who offer a combination of the skills, knowledge and experience listed below are encouraged to apply. With our continued growth we are hiring talent to join us on our journey and grow with us.

Sr CRAs require skills in planning and preparation; sourcing and collecting information; prioritizing tasks and actions; and displaying a proactive attitude to assist in project planning and study execution.

We seek -

  • B.A./B.S. or equivalent experience in a (para)medical, scientific or health related discipline or related work experience

  • Region base of PA, MD and/or New York to undertake regional travel across these regions.

  • Medical Device Experience Required

  • Therapeutic Preference: Medical Device / Respiratory / Cardiovascular.

  • Minimum 4 years of relevant CRA work experience, with extensive medical device monitoring experience.

  • Tracker and Start-up experience (with good spreadsheet or similar skills)

  • Ability to understand basic and complex medical details.

  • GCP-ICH-E6, FDA regulations and ISO 14155, 13485 and 9001 knowledge where applicable; knowledge of/ability to learn regulations and guidelines on medical devices and clinical trials.

  • Ability to travel up to 75% domestically and internationally.

  • Experience as a Clinical Lead helpful

  • Strong communicator with excellent presentation skills; able to build rapport with site personnel

We offer -

  • The opportunity to work in an innovative, fast-growing and rewarding industry

  • A dynamic and enthusiastic global team that fosters collaboration and the opportunity to work with experts across many specialties

  • Exchange of knowledge and ideas to help employees grow and advance their careers, backed with training and other development opportunities

  • Competitive compensation and benefits package (details shared during the interview process)

  • Some roles offer the opportunities for travel

  • Ask us about our hybrid and fully remote work opportunities

Avania - MedTech's trusted Champion

We look forward to receiving your application!

Avania takes pride in being an equal opportunity employer. We consider qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic.

#LI-DNI

How this job compares

Set against the 573 open Clinical Research Associate jobs on Olive Jobs, counted November 7, 2026.

Pay
  • This postingup to $140K/yr
  • US median$75–175K/yr218 salary ranges
  • US median$56–62/hr39 hourly ranges
Openings
Olive Jobs lists 573 open Clinical Research Associate jobs across the US. 24% of them nationwide are listed as remote or flexible.
Hiring the most across the US
Experience
This posting asks for at least 4 years of experience — more than three in four Clinical Research Associate postings that state a minimum ask for (median 2 years, across 507 postings).
Education
146 of the 573 open Clinical Research Associate jobs (25%) ask for a bachelor's degree or higher.

Counted across the open, public US postings on Olive Jobs on November 7, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.

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