Intern Cra

As a leading contract research organization (CRO), Labcorp Drug Development provides comprehensive drug development solutions for a range of industries. Our services cover the preclinical, clinical and post-market phases of drug development, the product life cycles for medical device and diagnostics and development services paired with regulatory support for the chemical testing and crop protection industries.

Joining our team will offer you a rewarding career, an opportunity to work in a high-energy, diverse and collaborative workplace. Your work as an intern will be meaningful. With the support of exceptional people, you’ll be empowered to start your career journey with mentoring, training and personalized development planning.

Labcorp Clinical Development is offering graduates a unique opportunity to be fully trained as a CRA as part of our **traineeship** Program.

**Responsibilities**:

- Assist CRAs with preparation for site visits (i.e. running reports, QC of files (checking for missing documents), resolving action items from previous visits).
- Assist with the coordination of study visits and shipment of drug, ancillary supplies, and laboratory kits/samples.
- Liaise with the project team and others to distribute and track clinical trial supplies, e.g. Case Report Forms, study medication, lab kits, ensuring that sites have sufficient supplies to continue recruitment
- Liaise with the CTA to assist the Project Team in the production of Status Reports.
- Assist in submissions and notifications to Ethics Committees and Regulatory Authorities as applicable in region
- Assist Clinical Research Associate MEA I, (CRA MEA I), InHouse Clinical Research Associate II (IHCRA II), Sr. In-House Clinical Research Associate (Sr. IHCRA), Clinical Research Associate 1 (CRA1), Clinical Research Associate 2 (CRA 2), Senior Clinical Research Associate 1 (Sr. CRA 1) and Senior Clinical Research Associate 2 (Sr. CRA 2) with on-site tasks as required and according to training goals (e.g. review of Case Report Forms, Site Regulatory File and drug accountability).
- Opportunity to perform remote visits (i.e. Phone PSVs, Phone SIVs, remote RMVs, remote COVs) as required by the monitoring plan.

**Education and Qualifications**:

- In process of obtaining a University 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
- Excellent language level both in French and English

We look forward to hearing from you.

**Did you know?**

**Labcorp is proud to be an Equal Opportunity Employer**:
As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.

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