Clinical Research Coordinator

3 weeks ago

Red Deer, Canada CARe Clinic Full time

**Clinical Research Coordinator**

Our Clinic consists of a network of medical clinics in the Central Alberta region, expanding our clinical trial expertise into many therapeutic areas. Our research staff are (inter)nationally recognized and well respected by top pharmaceutical and biotech companies for the high-quality care and superior data collected while patients participate in clinical trials undertaken by our team.

Currently, we are looking to add a Clinical Research Coordinator to our team who can work for us on a Part-time with the opportunity to grow the position into Full-Time.

**Responsibilities will include but are not limited to**:

- Provide overall care and educational support to patients and clinical trial participants
- Review referrals and medical histories and determine eligibility and suitability for clinical trial protocols based on assessment information
- Follow GCP, ICH guidelines and Clinic SOPs at all times
- Complete participant screening utilizing appropriate tools and clinic procedures; utilizing an advanced knowledge and skill in history and physical assessment
- Assess the clinical needs of the patient prior to presenting research options and determine a plan based on the assessment
- Adjust work schedules to integrate newly approved clinical trials into ongoing research activities
- Demonstrate professional behaviour when dealing with patients, their family, visitors, physicians, other health care providers and clinic staff
- Responsible for lab sample collection and processing
- Administration of study drug, study supplies, questionnaires, etc.
- Implement clinical study protocols, monitor daily study activities and progress and prepare reports/updates to investigators and management as appropriate.
- Monitor enrolment goals and modify recruitment strategies as necessary.
- Ensure that all clinical activities are carried out in accordance with established research protocols and standards in compliance with all applicable laws, regulations and policies including but not limited to GCP, ICH and Clinic SOPs
- Responsible for maintaining study regulatory study documents.
- Responsible for reporting of abnormal results, adverse and serious adverse events to the Investigator and Sponsor according to the study protocol and in accordance with local ethics board, regulatory agencies and sponsor requirements.
- Perform miscellaneous job-related duties as assigned.
- Schedule study participant visits as per protocol.
- Perform delegated protocol specific activities completely and accurately; vitals, ECGs, laboratory assessments, questionnaires, IP administration, etc.
- Obtain all necessary documentation as required by the protocol(i.e. medical history, hospital records, etc.)
- Create source documents and any other research documents required for the successful conduct of a clinical research study
- Meet with the Sponsor's representatives to discuss the conduct of the study and review study data; follow-up as required based on meeting/review.

**Requirements**:

- Strong knowledge of medical terminology; e.g. Medical Office Assistant, Lab Tech, RRT, etc
- Certified Clinical Research Coordinator (e.g. CCRP), preferred
- Phlebotomy experience preferred and considered an asset
- Capability to successfully manage multiple competing priorities with mínimal supervision and direction
- Exceptional communication and interpersonal skills are required
- Expertise in patient interviewing, counselling and teaching
- Demonstrate initiative, accountability, good time management, decision making ability and strong organizational skills
- Proficiency with MS Office including creating spreadsheets, reports and documents

We seek dynamic individuals who embrace opportunities for learning and innovation and those who contribute to the vision of providing quality care.

**Job Types**: Full-time, Part-time, Permanent

**Benefits**:

- Extended health care
- Flexible schedule
- On-site parking
- Paid time off

Schedule:

- 8 hour shift

Supplemental pay types:

- Overtime pay

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