Covance Clin Res Assoc II in Lima, Prince Edward Island

Job Overview

Are you ready to redefine what’s possible, and discover your extraordinary potential at Covance? A career here provides the unique chance to create a lasting impact and difference in our patient’s lives. Joining our team will offer you a rewarding career, an opportunity to work in a high-energy & collaborative workplace, along with access to comprehensive benefits. Your work will be meaningful, the patient outcomes are real, and the results are lasting. With the support of exceptional people from across the globe and an energized purpose, you’ll be empowered to own your career journey with mentoring, training and personalized development planning.

Our mission is to help our clients bring the miracles of medicine to market sooner -- join us for your next career move.

Education/Qualifications

Minimum Required:

External Candidates

o University or college degree, or certification in a related allied health profession from

an appropriately accredited institution (e.g., nursing licensure),

AND

o a minimum of 2 years of Clinical Monitoring experience.

 Internal Candidates

o 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:

External Candidates

o University or college degree, or certification in a related allied health profession

from an appropriately accredited institution (e.g., nursing licensure),

AND

o a minimum of 2 years of Clinical Monitoring experience.

 Internal Candidates

o 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 2018-26223

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.