Covance Clin Res Assoc II in Mexico

Job Overview

Cardiovascular, Vaccines, Dermatology, CNS and Respiratory.

AREAS OF EXPERTISE

 Phase I- III Protocols

 GCP/ICH

 EDC (Inform, OC-RDC, and Medidata-RAVE)

 CTMS (E-Clinical, ICOTrial)

 Microsoft Office Proficiency

 PSV, SIV, SMV and COV

EXPERIENCE

Education/Qualifications

Minimum Required:

¨ Position is located in Monterrey, Mexico

¨External Candidates

¨ University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure), AND

¨a minimum of 2 years of Clinical Monitoring experience.

¨Internal Candidates

¨Internal candidates with a minimum of 2 years of Clinical Monitoring experience

¨Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements

¨Thorough knowledge of monitoring procedures

¨Basic understanding of the clinical trial process

Preferred:

¨Thorough knowledge of Covance SOPs for site monitoring

Experience

Minimum Required:

¨ Position is located in Monterrey, Mexico

¨External Candidates

¨University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure), AND

¨a minimum of 2 years of Clinical Monitoring experience.

¨Internal Candidates

¨Internal candidates with a minimum of 2 years of Clinical Monitoring experience

¨Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines

¨Have a full understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs¨Good planning, organization and problem solving abilities

¨Ability to work with minimal supervision

¨Good communication and interpersonal skills

¨Good analytical and negotiation skills

¨Computer competency

¨Fluent in local office language and in English, both written and verbal

¨Works efficiently and effectively in a matrix environment

Preferred:

One (1) or more additional years of experience in a related field (i.e. medical, clinical, pharmaceutical, laboratory, research, data analysis, data management or technical writing) is preferred

Job Number 2018-19516

Job Category Clinical Research Associate

Position Type Full-Time

Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran/Sexual Orientation/Gender Identity). Your confidentiality and privacy are important to us.