Medical Assistant
2 months ago
**Pharma Medica Research** is a full service contract research organization specialized in conducting early phase clinical trials in healthy volunteers, special and patient populations. We are currently looking for a Nurse to join our clinic location in Scarborough.
The function of the Medical Assistant I is to ensure all investigational products are handled according to GCP guidelines and the Standard Operating Procedures (SOPs) of Pharma Medica Research Inc. (**_PMRI_**). Monitor the health and safety of volunteers throughout the conduct of clinical studies. The Medical Assistant I reports to the Manager, Clinical Operations and/or designate.
**Duties and Responsibilities**:
Responsibilities include but are not limited to:
1. Responsible for investigational product accountability at PMRI under the supervision of the investigator/institution.
2. Dispense/repackage and use the investigational products in accordance with the approved protocol.
3. Ensure that the investigational products are stored as specified by the sponsor and in accordance with applicable regulatory requirements.
4. Reconcile and archive investigational products at the completion of the study.
7. Administer investigational products (i.e. oral, subcutaneous, inhalations, nasal or any other non-invasive administration route) for the conduct of a clinical study with no injection, as well as any concomitant medication under the supervision/order of the investigator.
9. Perform study procedures as required (e.g. conducting ICFs, collecting samples if certified, and recording adverse events).
10. Maintain and document emergency drugs, products, and supplies in the clinic including crash cart, emergency medication, AED, etc.
11. Involved in Medical Emergency mock training.
13. Perform other study procedures (e.g. conduct various consents with volunteers, process samples, record adverse events, and assist Investigators etc.). Write and review Standard Operating Procedures (SOPs).
14. Oversee on-floor clinical activities together with the Group Leaders/Study Coordinators to ensure study procedures comply with protocol and SOPs.
15. Perform screening procedures such as but not limited to: blood sample collection, sample processing and storage, vital signs, ECGs, etc., according to the study protocol and/or SOP requirements, as required.
16. Ensure all duties are conducted in compliance with SOP, regulatory guidelines and applicable regulations.
17. Other duties as required.
**Qualifications**:
- Medical and/or nursing related training or certification.
- At least 3 years of medical related experience.
- General computer experience.
- Good communication skills including good English verbal and written skills.
- Good interpersonal and organizational skills.
- Ability to work both independently and as a team member.
- First Aid and CPR certification preferred.
- ACLS certification is an additional asset.
- Basic computer proficiency.
**We Offer**
- Competitive compensation plan
- Opportunities for advancement and career progression
- A generous Employee Milestones Awards Program
- Corporate Discounts Program
- Learning Support Programs
- Friendly atmosphere, culture of learning
**PMR**I is an Equal Opportunity Employer; promoting accessibility and inclusivity at work and offering accommodation for applicants as required and requested.
We thank all applicants for their interest; however, only those selected to proceed in the interview process will be contacted.
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