Clinical Research Associate II, Dermatology & Rheumatology CRO, USA, (NH, MA, RI
Indero (formerly Innovaderm), Portland, OR, United States
Clinical Research Associate II, Dermatology & Rheumatology, CRO, USA (NH, MA, RI, CT)
The Clinical Research Associate II (CRA II) 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, 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
Conduct 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.
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 their 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
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 Microsoft Office (Word, Excel, PowerPoint).
Experience in dermatology is an asset.
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 the United States.
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The Clinical Research Associate II (CRA II) 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, 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
Conduct 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.
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 their 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
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 Microsoft Office (Word, Excel, PowerPoint).
Experience in dermatology is an asset.
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 the United States.
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