
Clinical Trial Assistant
14 hours ago
The Clinical Trial Assistant (CTA) is responsible for providing project administrative support to the Clinical Operations team members including Clinical Research Associates (CRAs), Clinical Trial Managers (CTMs) and Central Monitors (CMs.)
**This role will be perfect for you if**:
- You have an experience in clinical research and you enjoy working with a Canadian-owned mid-sized CRO;
- You want to work in an administrative support-type of role;
More specifically, the Clinical Trial Assistant will:
- Assist Clinical Research Associates (CRAs), Clinical Trial Managers (CTMs), Central Monitors (CMs) and other Clinical Operations team members with generating reports from clinical systems such as the EDC, CTMS and TMF (e.g. reports on action items, protocol deviations, data entry and query status, source data verification status, etc.;)
- Assist with the periodic review of study files, training documentation and CTMS for completeness (e.g. eTMF, CRA calendar, project and systems training completion) and verifies that action items and protocol deviations have been pushed from the site visit reports to the CTMS library;)
- Review CTMS to verify CRA site assignments are up to date and accurate;
- Assist with the tracking of visits, site visit report compliance, and study documents;
- Attend Clinical Operations project team meetings and take minutes;
- May assist in the preparation, distribution, and filing of clinical documents and study supplies;
- May perform central monitoring activities.
**Requirements**:
**Education**
- Highshool or secondary diploma;
**Experience**
- Experience in clinical research in the biotechnology, pharmaceutical, and/or CRO industry an asset;
- At least 1 year of experience working in an administrative support-type of role;
**Knowledge and skills**
- Ability to work in a fast-paced evolving and global environment and establish good relationships with colleagues and sites;
- Strong organizational, communication, problem-solving, time management and multi-tasking skills;
- Attention to detail and accuracy in work.
- Strong mastery of Microsoft Office suite (Word, Excel, Power Point);
- Good written and verbal skills in English;
Our company:
**The work environment**
At Innovaderm, you will work with brilliant and driven colleagues. Our values are collaboration, innovation, reliability and responsiveness. We offer a stimulating work environment and attractive advancement opportunities.
In this position, you will be eligible for the following perks:
- Flexible schedule
- Vacation
- Home-based position
- Ongoing learning and development
**About Innovaderm**
Innovaderm is a contract research organization (CRO) specialized in dermatology. Since its beginnings in 2000, our organization has benefited from a solid reputation for the quality of its research and services exceeding the expectations of its clients. Based in Montreal, Innovaderm continues to grow and expand in North America and Europe.
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