About the Company
Pemberton BioResearch Solutions is a dynamic and emerging Contract Research Organization (CRO) based in beautiful Pemberton, British Columbia. We specialize in supporting small to mid-sized biotech and pharmaceutical companies through the complex landscape of clinical trial management and regulatory compliance. Our mission is to accelerate medical innovation by providing meticulous and ethical research services, fostering a collaborative environment, and nurturing the next generation of industry professionals. Join our growing team and contribute to advancements in healthcare.
Job Description
We are seeking a highly motivated and enthusiastic Clinical Trials & Regulatory Affairs Intern to join our dedicated team. This entry-level internship offers a unique opportunity to gain hands-on experience in the critical areas of clinical research and regulatory compliance within a professional CRO setting. No prior experience in clinical trials or regulatory affairs is required; we are looking for individuals eager to learn, grow, and contribute. You will receive comprehensive training and mentorship, working alongside experienced professionals to understand the intricacies of drug development and regulatory submissions.
Key Responsibilities
- Assist in the preparation, review, and maintenance of regulatory documents and submissions (e.g., EC/IRB submissions, CTAs).
- Support the clinical operations team with trial master file (TMF) management, ensuring all essential documents are current and compliant.
- Conduct literature searches and data compilation to support clinical study design and regulatory strategy.
- Participate in internal meetings related to clinical trial planning, execution, and regulatory updates.
- Learn about Good Clinical Practice (GCP) guidelines and apply them to daily tasks.
- Help with quality control checks of study documents and databases.
- Contribute to the development and improvement of internal standard operating procedures (SOPs).
- Perform general administrative duties to support the Clinical Operations and Regulatory Affairs departments.
Required Skills
- Strong interest in clinical research, life sciences, or healthcare.
- Excellent organizational and time management skills.
- Meticulous attention to detail and accuracy.
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
- Strong verbal and written communication skills.
- Ability to work independently as well as part of a team.
- Eagerness to learn and adapt in a fast-paced environment.
Preferred Qualifications
- Currently enrolled in or recently graduated from a Bachelor's or Master's degree program in Life Sciences, Pharmacy, Nursing, Public Health, or a related field.
- Basic understanding of medical terminology or biological processes.
- Previous experience with data entry or document management (academic or professional).
Perks & Benefits
- Hands-on experience in a real-world CRO environment.
- Mentorship from experienced professionals in clinical trials and regulatory affairs.
- Opportunity to contribute to impactful medical research.
- Exposure to various phases of drug development.
- Networking opportunities within the biotech and pharma industries.
- Potential for future full-time employment based on performance.
- Professional development workshops and training sessions.
How to Apply
If you are interested in this position, please click the "Apply Now" button below. To ensure your application is properly considered, please prepare the following:
- An up-to-date Resume or CV
- A brief cover letter summarizing your experience and motivation
Applications are reviewed on a rolling basis. Only shortlisted candidates will be contacted for an interview.
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