Overview
Si desea conocer los requisitos para este puesto, siga leyendo para obtener toda la información relevante.
Freelance / Contractual Clinical Research Associate (cCRA) with experience in Dermatology, Spain. The Contractual CRA will monitor the progress of clinical studies at investigative sites or remotely, ensuring trials are conducted, recorded, and reported in accordance with the protocol, SOPs, ICH-GCP, and all applicable regulatory requirements.
Ideal Candidate
Experienced CRA with the ability to work autonomously to meet quality standards and deadlines
Interested in dermatology and developing expertise in this therapeutic area
Enjoys working for a mid-sized CRO where contributions are noticed and valued
Responsibilities
Conduct site qualification, initiation, monitoring, and close‑out visits for research sites according to the monitoring plan, Indero and sponsor SOPs, ICH/CGP guidelines and applicable regulations
Participate in investigators’ meetings
Prepare site visit reports and follow‑up letters to the investigator
Build productive relationships with investigators and site staff to achieve study objectives, including patient recruitment targets
Perform source data verification, ensure 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 the former description, if they have the required experience, are qualified and/or have received adequate training
Requirements
Education:
B.Sc. in a field relevant to clinical research, nursing degree and/or equivalent experience
Experience:
3 years of experience in conducting on‑site clinical monitoring in the biotechnology, pharmaceutical, and/of CRO industry; at least 1 year in dermatology
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 Microsoft Office (Word, Excel, PowerPoint); experience in dermatology is an asset
EEO Statement
Indero is committed to providing equitable treatment and equal opportunity to all individuals. Indero will provide accommodations throughout the recruitment and selection process to applicants with disabilities, upon request. xpzdshu Indero only accepts applicants who can legally work in Spain.
#J-18808-Ljbffr