Job Title
Clinical Research Associate
Job Description
Clinical Research Associate (CRA), Sleep and Respiratory Care
This position supports clinical research trials by adhering to regulations, Philips procedures, and good clinical practice (GCP).
Please note: Due to the consolidation of our sites, this role will start at the Bakery Square office in Pittsburgh, Pennsylvania and will move to another site in the greater Pittsburgh area by the end of the year. This change will bring our teams in western Pennsylvania closer together to remain competitive and committed to our customers, clinicians, and patients and create value with sustainable impact.
Your role:
• The CRA executes site initiation, monitoring, and close-out visits, and identifies potential risks, and implements corrective actions to address deviations and non-compliance. The CRA will be expected to travel up to 25% to sites in the event remote monitoring is not an option.
• The CRA interacts with study stakeholders and tracks study progress against milestones and budgetary constraints via Clinical Trial Management System (CTMS).
• The CRA provides support and guidance to study sites and investigators on protocol requirements.
• This position will report into the Director of Clinical Operations for Sleep and Respiratory Care (SRC). The CRA will be required to report to the Pittsburgh office in a hybrid manner.
• Communicate and work effectively in a team and across a diverse global network of businesses/business partners and be comfortable in a virtual environment.
You’re the right fit if:
• You’ve acquired 2+ years of experience in clinical research, including experience with monitoring
• Your skills include knowledge with GCP, CTMS, Trial Master Files, Monitoring
• You have a Bachelor’s Degree in a science related field and/or relevant experience in clinical research
• You must be able to successfully perform the minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this Clinical position.
• You’re comfortable communicating, presenting, and following good ethical and clinical guidelines. You are willing to pivot as needed for priorities and to seek out training, as applicable.
• Ability to manage device shipping/receiving and may require lifting up to 25 pounds
About Philips
We are a health technology company. We built our entire company around the belief that every human matters, and we won’t stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.
• Learn more about our business.
• Discover our rich and exciting history.
• Learn more about our purpose.
• Read more about our employee benefits.
If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our commitment to diversity and inclusion here.
Additional Information
US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.
Company relocation benefits will not be provided for this position. For this position, you must reside in or within commuting distance to Pittsburgh, PA, USA. (Bakery Square, Murrysville and New Kensington)
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This requisition is expected to stay active for 45 days but may close earlier if a successful candidate is selected or business necessity dictates. Interested candidates are encouraged to apply as soon as possible to ensure consideration.
Philips is an Equal Employment and Opportunity Employer/Disabled/Veteran and maintains a drug-free workplace.
Tagged as: Research associate