Clinical Research Nurse I
About The Position
At Altasciences, we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences. We are better together and together We Are Altasciences. The Clinical Research Nurse II will oversee the safety and consent of clinical trial participants during study conduct and the maintenance of safety equipment. The Clinical Research Nurse II will execute tasks performed in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs). Work Schedule: Evenings/Overnight
Requirements
- Degree from accredited Registered Nurse program required or bachelor’s degree in nursing from an accredited school.
- Minimum of 4+ years of related clinical research experience required.
- Current Registered Nurse (RN) license, required
- Current Basic Life Support (BLS, CPR/AED) certification, required
- Current Advanced Cardiac Life Support (ACLS) certification, required
- Ordre des infirmières et infirmiers du Québec (OIIQ) permit
- Cardiopulmonary resuscitation (CPR) certification, required.
- Advanced Cardiovascular Life Support (ACLS) certifications, required
- Microsoft suite
- Strong computer literacy
- Ability to read and interpret technical documents and industry specific manuals.
- Ability to write advanced reports and correspondence.
- Ability to speak effectively before groups of customers or employees of the organization.
- Excellent verbal and written communication skills.
- Well-developed interpersonal skills are required.
- Personal/professional integrity and proven discretion in handling confidential information.
- Capable of managing multiple conflicting priorities.
Nice To Haves
- Bilingual proficiency in French may be required, depending on location.
- Relevant industry experience a plus.
Responsibilities
- Perform scheduled inspection of emergency crash carts, inventory/inspect the contents, and maintain up to date records.
- May train employees on clinical trial activities associated to their job’s needs.
- Ensure the confidentiality of clinical trial participants and sponsors is respected.
- Perform clinical trial activities including but not limited to, continuous safety monitoring, safety assessments, Investigational Product (IP) administration and catheter installation.
- Monitor, document and/or follow-up on participant adverse events.
- Maintain and advocate a high level of patient care, quality, and safety within the department.
- May assist in study related consenting with participant screenings.
- Provide feedback, where necessary, to appropriate team members of study progress.
- Proactively communicate issues and/or problem resolutions to departmental supervisors and managers.
- Other tasks as assigned by management
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Mid Level
