# Experienced Clinical Research Associate (CRA II / SR CRA) - US East Region (Northeast & Southeast) - Multiple Therapeutic Areas Available [Thermo Fisher](https://www.jorb.ai/firms/thermo-fisher.md) · New York · United States Thermo Fisher is hiring a Experienced Clinical Research Associate (CRA II / SR CRA) - US East Region (Northeast & Southeast) - Multiple Therapeutic Areas Available in New York. Posted 2026-07-15; applications close 2026-09-13. **Apply**: https://jobs.thermofisher.com/global/en/job/TFSCGLOBALR01354148EXTERNALENGLOBAL/experienced-clinical-research-associate-(cra-ii-/-sr-cra)---us-east-region-(northeast-&-southeast)---multiple-therapeutic-areas-available Posted 7d ago. ## Role details ## Work Schedule Standard (Mon–Fri) ## Environmental Conditions Office ## Job Description **Join Us as a Clinical Research Associate (Level II)** – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last five years. As part of our global team, you’ll perform and coordinate clinical monitoring and site management activities. As a Clinical Research Associate (Level II), you will conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation. You will manage procedures and guidelines from different sponsors and/or monitoring environments (e.g., FSO, FSP, Government, etc.). Acting as a site process specialist, you will ensure the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects’ rights, well-being, and data reliability. You will ensure audit readiness and develop collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to your role are outlined in the task matrix. ## Education and Experience Requirements - Bachelor’s degree in a life science related field, or a Registered Nursing certification, or equivalent and relevant formal academic/vocational qualification. - Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 1 year as a clinical research monitor), or completion of a PPD Drug Development Fellowship. - Valid driver’s license where applicable. - 1–2 years of traveling on-site monitoring experience is required. - Therapeutic experience in at least one of the following areas: Oncology, Ophthalmology, Neurology, Cardiology, Rare Disease, Respiratory, Obesity, and/or Pulmonary. - Candidates must live within 60 miles of the nearest major airport. Up to 80% travel is expected. - Must be legally authorized to work in the United States without sponsorship. - Must be able to pass a comprehensive background check, including a drug screening. ## Knowledge, Skills, and Abilities - Proven clinical monitoring skills. - Demonstrated understanding of medical/therapeutic area knowledge and medical terminology. - Demonstrated ability to attain and maintain a working knowledge of ICH GCPs, applicable regulations, and procedural documents. - Well-developed critical thinking skills, including critical mindset, in-depth investigation for appropriate root cause analysis, and problem solving. - Ability to manage Risk Based Monitoring concepts and processes. - Good oral and written communication skills, with the ability to communicate effectively with medical personnel. - Ability to maintain customer focus through good listening skills, attention to detail, and the ability to perceive customers’ underlying issues. - Good organizational and time management skills. - Effective interpersonal skills. - Attention to detail. - Ability to remain flexible and adaptable in a wide range of scenarios. - Ability to work in a team or independently as required. - Good computer skills: solid knowledge of Microsoft Office and the ability to learn appropriate software. - Good English language and grammar skills. - Good presentation skills. ## Working Conditions and Environment - Work is performed in an office/laboratory/clinical and/or home office environment with exposure to electrical office equipment. - Frequent drives to site locations. Frequent travel, generally 60–80% (and more for some individuals). May also include extended overnight stays. - Exposure to biological fluids with potential exposure to infectious organisms. - Personal protective equipment required such as protective eyewear, garments, and gloves. - Exposure to fluctuating and/or extreme temperatures on rare occasions. ## Compensation and Benefits The salary range estimated for this position based in Florida is **$85,000.00–$130,000.00**. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that includes: - A choice of national medical and dental plans, and a national vision plan, including health incentive programs. - Employee assistance and family support programs, including commuter benefits and tuition reimbursement. - At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy. - Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan. - Employees’ Stock Purchase Plan (ESPP), offering eligible colleagues the opportunity to purchase company stock at a discount. For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards ## Applying to this role This Experienced Clinical Research Associate (CRA II / SR CRA) - US East Region (Northeast & Southeast) - Multiple Therapeutic Areas Available role at Thermo Fisher runs through the firm's own careers portal and expects a CV and cover letter written specifically for the posting, not a portable submission carried across firms. Jorb AI's application agent tailors a CV and cover letter from your background to this posting and tracks the role alongside the rest of your applications. [Tailor this application](https://www.jorb.ai/signup?ref=job-atom&firm=thermo-fisher&job=6a58598653c584effa43eecc) ## More open roles at Thermo Fisher - [Manufacturing Technician II - 2nd shift](https://www.jorb.ai/jobs/6a5ac43353dd8be283d04447.md) – New York, posted 5d ago - [Manufacturing Technician II - 3rd Shift](https://www.jorb.ai/jobs/6a5ac43353dd8be283d04442.md) – New York, posted 5d ago - [Document Control Administrator II - 1st Shift](https://www.jorb.ai/jobs/6a5ac43353dd8be283d04448.md) – New York, posted 5d ago - [Microbiologist I (Normal Office Hours initially | Future 12 Rotating Shift Opportunity)](https://www.jorb.ai/jobs/6a57789db32a30f0c91fd940.md) – Singapore, posted 7d ago - [Operator II, Manufacturing - 2nd Shift](https://www.jorb.ai/jobs/6a5707f44074dcae6dabe5a8.md) – New York, posted 8d ago --- Updated: 2026-07-22 Canonical: https://www.jorb.ai/jobs/6a58598653c584effa43eecc