Assistant(e) de recherche / Research Assistant - North Vancouver, British Columbia

IQVIA LLC; Vancouver; On-site; CAD 40,000 - 60,000; Part time

Job summary

A global leader in clinical research located in Vancouver is seeking a Research Assistant to support clinical study activities. The successful candidate will have strong interpersonal skills and experience in data entry. A Bachelor’s degree in life sciences or a related field, or relevant clinical research experience, is required. This part-time role offers a chance to be involved in significant healthcare advancements.

Qualifications

• 2 years of experience in clinical research, or 3 years with a high school diploma.
• Practical knowledge of clinical studies and data entry in EDC.
• Understanding of Good Clinical Practice (GCP) principles.

Responsibilities

• Data entry and query resolution in EDC.
• Develop and maintain effective communication with study team members.
• Assist in participant recruitment and screening.

Skills

Logical thinking

Prioritization

Adaptability

Interpersonal skills

Teamwork skills

Education

Bachelor's degree in life sciences or related field

High school diploma with relevant experience

Job description

Title: Assistant(e) de recherche / Research Assistant - North Vancouver, British Columbia

Location: Vancouver, British Columbia, Canada

Work type: Part time

Posted on: Yesterday

Job Requisition ID: R1492307

Job Summary

This role involves supporting clinical study activities in compliance with applicable regulations. Key skills include logical thinking, prioritization, adaptability, and strong interpersonal and teamwork skills.

Responsibilities

1. Data entry and query resolution in EDC
2. Develop and maintain effective communication with study team members
3. Build trust and respect with investigators and site staff
4. Assist in participant recruitment and screening
5. Coordinate patient scheduling and follow-up procedures
6. Collect patient history and manage follow-up care and lab procedures
7. Adhere to approved protocols and assist with informed consent process
8. Ensure participant safety and coordinate protocol-related procedures and visits
9. Follow company policies, SOPs, and guidelines

Qualifications

1. Bachelor's degree in life sciences or related field with 2 years of experience, or high school diploma with 3 years of relevant clinical research experience
2. Practical knowledge of clinical studies and data entry in EDC
3. Understanding of Good Clinical Practice (GCP) principles
4. Knowledge of study protocols, consent forms, and study calendars
5. Ability to perform required clinical procedures and understand medical terminology
6. Attention to detail and effective communication skills
7. Applicable certifications and licenses as required

IQVIA is a global leader in clinical research services, commercial insights, and healthcare intelligence, dedicated to accelerating the development of innovative treatments. For more information, visit https://jobs.iqvia.com

IQVIA is an equal opportunity employer. All qualified applicants will be considered without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, marital status, or other protected statuses. Accommodations are available upon request for candidates with disabilities. Please contact us at [e-mail].

Note

We may use AI in processing applications solely to assist the recruitment process, not to replace human decision-making.

Job Reference: J-18808-Ljbffr