Senior Clinical Research Associate / Clinical Research Associate II, Poland (dermatology and rheumatology CRO)
The Clinical Research Associate II (CRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.
This role will be perfect for you if :
- 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
RESPONSIBILITIES
The clinical research associate (CRA) :
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 regulationsParticipates in investigators’ meetingsPrepares site visit reports and follow-up letters to the investigatorBuilds productive relationships with investigators and site staff to achieve study objectives, including patient recruitment targetsPerforms source data verification, ensures on-site study drug storage, dispensing, and accountability, data collection, and regulatory document collection is adequateOur company : The work environment
At 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.
In this position, you will be eligible for the following perks :
Permanent full-time positionVacation, PPK, health allowanceHome-based position with teleworking allowanceOngoing learning and developmentWork location
This position is opened to candidates across Poland (home-based position).
Recruitment process : what to expect
As part of the recruitment process for this position you will meet various team members at InderoThe first interview will be conducted by Teams (20 minutes) and the second via video conference ( Teams 1 hour)About Indero
Indero is a contract research organization (CRO) specialized in dermatology and rheumatology. Since its beginnings in 2000, our organization has benefited from a solid reputation for the quality of its research and services exceeding the expectations of its clients. Based in Montreal, Indero continues to grow and expand in North America and Europe.
Indero is committed to providing equitable treatment and equal opportunity to all individuals. As such, Indero will provide accommodations throughout the recruitment and selection process to applicants with disabilities, upon request.
Indero only accepts applicants who can legally work in Poland.
Education
B.Sc. in a field relevant to clinical research, nursing degree and / or equivalent experienceExperience
2 to 5 years experience in conducting on-site clinical monitoring in the biotechnology, pharmaceutical, and / or contract research organization (CRO) industryKnowledge and skills
Good knowledge of ICH / GCP standards and applicable regulatory requirementsStrong verbal and written communication skills in EnglishAbility to prioritize different assignments and work under pressure while maintaining attention to detail and meeting timelinesExcellent judgement and problem-solving skillsTravel to research sites approximately 65% of the timeExcellent knowledge of Microsoft Office (i.e., Word, Excel, PowerPoint)Experience in dermatology is an asset