About the Company
IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. With a global network spanning more than 100 countries, IQVIA is committed to advancing human health by creating innovative solutions to improve clinical development and commercialization.
Job Description
We are seeking enthusiastic and driven individuals to join our team as Summer Clinical Research Interns. This internship offers a unique opportunity to gain hands-on experience in the dynamic field of clinical research, working alongside seasoned professionals on various projects aimed at accelerating the development of life-changing therapies. Interns will contribute to critical aspects of clinical trial operations, data management, and regulatory compliance within a world-class research environment.
Key Responsibilities
- Assist in the preparation and review of study-related documents, including protocols, informed consent forms, and case report forms.
- Support clinical trial management activities, such as site initiation, monitoring, and close-out procedures.
- Contribute to data collection, entry, and quality control processes to ensure accuracy and integrity of clinical data.
- Participate in team meetings and contribute to discussions on study progress, challenges, and solutions.
- Conduct literature reviews and assist with research projects as assigned.
- Adhere to Good Clinical Practice (GCP) guidelines and all relevant regulatory requirements.
- Collaborate effectively with cross-functional teams, including clinical operations, data management, and regulatory affairs.
Required Skills
- Currently enrolled in a Bachelor's or Master's degree program in a life science, health science, public health, or related field.
- Strong interest in clinical research and drug development.
- Excellent written and verbal communication skills.
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
- Ability to work independently and as part of a team.
- Strong attention to detail and organizational skills.
- Legally authorized to work in Canada for the duration of the internship.
Preferred Qualifications
- Previous exposure to clinical research concepts or coursework.
- Familiarity with medical terminology.
- Experience with statistical software or databases.
- GPA of 3.0 or higher.
Perks & Benefits
- Opportunity to gain practical experience in a global leader in clinical research.
- Mentorship from experienced professionals.
- Exposure to various phases of clinical trials.
- Networking opportunities within the life sciences industry.
- Professional development workshops and learning resources.
- Competitive hourly wage.
How to Apply
Interested candidates are invited to submit their application by clicking the "Apply Now" button below. To ensure your application is considered, please include the following:
- A current resume
- A cover letter outlining your suitability for the role and your motivation for applying.
We review applications on a rolling basis and will contact shortlisted candidates for an interview.
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