Covance Clin Res Assoc I in Mexico City, Mexico
Are you an organized person who can work independently and take ownership of your career? Would you like to gain on-the-job skills while helping advance life-changing medicines?
If you are looking to enter a nurturing environment that provides a clear path to advancement, consider furthering your career as a Covance Clinical Research Associate (CRA). In this role, you will:
Support large, prominent pharmaceutical companies with their clinical trials
Oversee site monitoring responsibilities with remote and in-person visits
Work in a flexible environment with a close-knit team
Use time management and people skills to ensure compliance
University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology).
Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements.
Thorough knowledge of monitoring procedures.
Thorough understanding of the clinical trial process.
Ability to monitor study sites independently according to protocol monitoring guidelines, S.O.P.s, 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.
Fluent in local office language and in English, both written and verbal.
Works efficiently and effectively in a matrix environment
- 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 2018-23614
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.