Clinical Research Associate II, Dermatology & Rheumatology, Canada (AB,MB)
Indero
- Montreal, QC
- Permanent
- Full-time
- You are an experienced CRA with a demonstrated ability to work autonomously to meet quality 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
- Conducts site qualification, initiation, monitoring, and close-out visits 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 achieve study objectives, including patient recruitment targets
- Performs source 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 description, if they have the required experience, are qualified and/or have received adequate training
InderoOur company:The work environmentAt Indero, you will work with brilliant 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 Indero
- The first interview will be conducted by Teams (30 minutes) and the second via video conference (1 hour)
- B.Sc. in a field relevant to clinical research, nursing degree and/or equivalent experience
- CRA for 2-5 years experience in conducting on-site clinical monitoring in the biotechnology, pharmaceutical, and/or contract research organization (CRO) industry
- 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 Microsoft Office (i.e., Word, Excel, PowerPoint)
- Experience in dermatology is an asset