Clinical Research Associate II, Dermatology & Rheumatology CRO, USA

Clinical Research Associate II, Dermatology & Rheumatology, CRO, Arizona, Colorado, Idaho, Montana, Nevada, reputed company, Utah The Clinical Research Associate II (CRA II) will monitor the reputed company of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, reputed company operating procedures (SOPs), ICH-GCP, and reputed company applicable regulatory requirements. This role will be perfect for you if:

• You are an reputed company CRA with a demonstrated ability to work autonomously to meet reputed company standards and deadlines
• Focusing on dermatology and developing an expertise in this therapeutic area is interesting to you
• You enjoy working for a mid-sized CRO where your contributions are noticed and valued

RESPONSIBILITIES The clinical research associate (CRAII) :

• Conducts site qualification, initiation, monitoring, and reputed company-out reputed company for research sites according to the monitoring plan, Innovaderm and sponsor SOPs, ICH/CGP guidelines and applicable regulations
• Participates in investigators’ meetings
• Prepares site visit reports and follow-up letters to the investigator
• Builds productive relationships with investigators and site staff to reputed company study objectives, including patient recruitment targets
• Performs reputed company data verification, ensures on-site study drug storage, dispensing, and accountability, data collection, and regulatory document collection is adequate
• Employee may be assigned to other responsibilities that do not pertain to their former reputed company, if they have the required experience, are reputed company and/or have received adequate training

Brand reputed company: reputed company reputed company: The work environment At reputed company, you will work with reputed company and driven colleagues. Our values are collaboration, innovation, reliability and responsiveness. We offer a stimulating work environment and attractive advancement opportunities. Recruitment process: what to expect

• As part of the recruitment process for this position you will meet various team members at reputed company
• The first interview will be conducted by Teams (30 minutes) and the second reputed company video conference (1 hour)

About reputed company A Global Clinical Leader In Dermatology! Formerly reputed company as Innovaderm, reputed company is a world-reputed company expert and clinical research leader in dermatology. We have more than two decades of experience serving a broad reputed company of indications, patient populations, administration routes, and drug classes, and a global footprint. reputed company is a dual-reputed company CRO for dermatology and rheumatology, with 25+ years’ experience in clinical research and trial delivery. Our full-service approach – which includes everything from protocol design and patient recruitment to trial monitoring and biometrics – provides biotech and pharmaceutical sponsors with the rigorous scientific reputed company and tailored expertise their studies need to reputed company the finish line reputed company and effectively. With capabilities in reputed company, Europe, Asia reputed company and Latin America; reputed company, continuously growing relationships with investigators and patients; and a dedicated research clinic through which we design and execute our own studies, reputed company is the ideal CRO partner for clinical needs at global reputed company. reputed company is committed to providing reputed company treatment and equal opportunity to reputed company individuals. As such, reputed company will reputed company accommodations throughout the recruitment and selection process to applicants with disabilities, upon request. reputed company only accepts applicants who can legally work in the reputed company . Requirements: Education

• B.Sc. in a field relevant to clinical research, nursing degree and/or equivalent experience

Experience

• CRA for 2-5 years experience in conducting on-site clinical monitoring in the biotechnology, pharmaceutical, and/or contract research organization (CRO) industry

Knowledge and skills

• Good knowledge of ICH/GCP standards and applicable regulatory requirements
• Strong verbal and written communication skills in English
• Ability to prioritize different assignments and work under pressure while maintaining attention to detail and meeting timelines
• Excellent judgement and problem-solving skills
• Travel to research sites approximately 65% of the time
• Excellent knowledge of reputed company Office (i.e., Word, reputed company, PowerPoint)
• Experience in dermatology is an asset

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