Clinical Research Associate

**Why Work for us?**

At Virogin Biotech, every day we strive to achieve incredible progress by working together to pursue our shared mission in developing novel oncolytic immunotherapies/mRNA vaccines and improving the lives of our patients. With our vision to be a global, best-in-class oncolytic virus company and with our patients’ welfare always at the top of our priorities, our teams work together to create impactful drugs for cancer patients with the hope of solving one of the world’s biggest challenges - a future without cancer.

**Position Overview**

With this opportunity, you’ll join a team of diverse and dedicated problem solvers, continuously challenging each other to bring forward diverse perspectives and insights that ignite innovation and make a difference to the work that we do. We are seeking a highly motivated professional who is looking to grow their career with our company.

**Responsibilities and work you’ll be part of**
- Support daily clinical study activities in the collection of documents from sites as needed during a study start-up, enrollment and close-out
- Filing of documents in TMF and conduct periodic review for completeness
- Assist the clinical team with accurate updating and maintenance of clinical documents and systems
- Assist with distribution and collection of Confidential Disclosure Agreements (CDAs) and prepare Investigator Site Files (ISFs)
- Schedule and take minutes of trial team meetings, review invoices from vendors and other trial tasks as needed
- Prepare, handle, and distribute clinical trial supplies and maintenance of tracking information
- Assist the clinical team with the preparation, distribution, filing and archiving of documentation and reports, according to the scope of work and Standard Operating Procedures (SOPs)
- Track and manage e-Case Report Forms (eCRFs), queries and clinical data flow
- Act as a project central contact for the clinical team communications and correspondence
- May be required to attend occasional site visits to assist with clinical monitoring duties

**Experience and Skills you’ll bring to the role**
- Bachelor’s Degree in Life Sciences
- Minimum 1 year experience in clinical research
- Minimum 3 years of administrative support experience
- Awareness of applicable clinical research regulatory requirements, Good Clinical Practices (GCP) & International Conference on Harmonization (ICH) guidelines
- Excellent computer skills including working knowledge of MS Office
- Proficient verbal and written communication skills in English
- Effective time management and organizational skills
- Strong attention to detail and problem-solving abilities

**The following experiences or abilities are assets**
- Experience working with Sponsor Company
- Knowledge in medical terminology

**Working conditions**
- Option for Hybrid or Remote working, and will need to work flexible work hours
- Works with mínimal supervision

**Salary**: From $55,000.00 per year

**Benefits**:

- Casual dress
- Dental care
- Extended health care
- Flextime
- Life insurance
- On-site parking
- Paid time off
- Vision care
- Work from home

Schedule:

- Monday to Friday

Supplemental pay types:

- Bonus pay

COVID-19 considerations:
COVID-19 vaccination is an employment requirement; accommodations will be considered upon request.

**Education**:

- Bachelor's Degree (required)

**Experience**:

- Clinical Research: 1 year (required)
- Administrative Support: 3 years (required)
- Good Clinical Practices (GCP): 1 year (required)
- International Conference on Hrmoniztion (ICH): 1 year (required)
- Working with Sponsor Company: 1 year (preferred)