Careers

Description

Bluewater Clinical Research is the largest clinical research organization in Canada. We have a long history of successful clinical studies that have contributed to the advancement of treatments for many medical conditions. And are team is growing! We are currently looking for a Research Facilitator who will be responsible for finding eligible patients for on going clinical studies. This includes generating leads, soliciting patients, facilitating recruitment and maintaining a patient database. The Research Facilitator is a positive and friendly representative of our organization who has excellent interpersonal and communication skills. They are outgoing, approachable, responsive and highly organized.

Key Responsibilities

• Recruit, schedule and follow-up with study participants.
• Complete relevant documentation regarding participant enrollment.
• Perform administrative duties such as: answering phones, booking appointments, etc.
• Responsible for safe management, cleanliness of the workspace

Employment and Education Requirements

• Healthcare experience including, but not limited to, working in primary care/family medicine office or other forms of healthcare experience/education
• Medical Terminology
• Advanced ability to use Microsoft Office programs

Reach out to info@bwresearch.ca

Description

Bluewater Clinical Research Group is seeking a full-time Clinical Research Coordinator.

The Clinical Research Coordinator meets with study subjects to guide them through the clinical trial process. The Clinical Research Coordinator is responsible for measuring vital signs, completing diagnostic studies and maintaining meticulous documentation, while adhering to the strict protocol procedures as outlined by the clinical research sponsor.

Basic Requirements

• Experience in a medical setting with a strong understanding of medical terminology
• Attention to detail and productive organizational skills
• Ability to work well under pressure and to exercise discretion and excellent judgment skills
• Demonstration of ability to follow protocols
• Interpret diagnostic tests (labs, x-rays, ultrasounds, etc.)
• Provide health teaching and extensive information regarding clinical studies
• Keep all patient information private and confidential
• Must thrive in a fast paced, multitasking environment
• Excellent interpersonal, verbal and written communication skills
• Must be a team player

Conduct of Research/Administrative

• Reviews and develops a familiarity with the protocol
• Assists Principal Investigator in communication of study requirements to all individuals involved in the study.
• Provides appropriate training and tools for study team members.
• Documents date of training and signatures of study personnel trained on study specific training log
• Collects documents needed to initiate the study and submit to the sponsor
• Works with the Principal Investigator to develop and implement recruitment strategies in accordance with requirements and approvals.
• Conducts informed consent processes
• Screens subjects for eligibility
• Coordinates participant medical tests and procedures.
• Collects data as required by the protocol
• Maintains study timelines.
• Maintains adequate inventory of study supplies
• Retains all study records in accordance with sponsor requirements, policies and procedures.
• Maintains effective and ongoing communication with sponsor, research participants and Principal Investigator during the course of the study.
• Assists Principal Investigator in preparation of any modifications to the scientific protocol in accordance with Federal regulations and sponsoring agency policies and procedures.

Required Experience, Skills and Abilities

• 3+ years of medical setting experience preferred
• Good leadership, problem solving and decision making skills are required.
• Demonstrated experience with Microsoft programs
• Strong critical thinking, teamwork and leadership skills
• Ability to function in a fast-paced and rapidly changing environment with openness to new ideas and the flexibility to adapt positively to changes in direction, priorities, schedules, or responsibilities
• Excellent time management skills with the ability to meet timelines
• Experience with the use of clinical databases or EMR systems
• Proficient in English with strong written and oral communication skills
• Proficient with Microsoft office suite (Excel, Word, Power Point)

Reach out to info@bwresearch.ca

Description

Bluewater Clinical Research Group is seeking a full-time Registered Practical Nurse.

The Clinical Research RPN is responsible for measuring vital signs, completing diagnostic studies and maintaining meticulous documentation, while adhering to the strict protocol procedures as outlined by the clinical research sponsor.

Basic Requirements

• Experience in a medical setting with a strong understanding of medical terminology
• Attention to detail and productive organizational skills
• Ability to work well under pressure and to exercise discretion and excellent judgment skills
• Demonstration of ability to follow protocols
• Interpret diagnostic tests (labs, x-rays, ultrasounds, etc.)
• Provide health teaching and extensive information regarding clinical studies
• Keep all patient information private and confidential
• Must thrive in a fast paced, multitasking environment
• Excellent interpersonal, verbal and written communication skills
• Complete lab draws, EKG, Infusions etc. in keeping with the specific clinical trial
• Must be a team player

Conduct of Research/Administrative

• Reviews and develops a familiarity with the protocol
• Assists Principal Investigator in communication of study requirements to all individuals involved in the study.
• Provides appropriate training and tools for study team members.
• Documents date of training and signatures of study personnel trained on study specific training log
• Collects documents needed to initiate the study and submit to the sponsor
• Works with the Principal Investigator to develop and implement recruitment strategies in accordance with requirements and approvals.
• Conducts informed consent processes
• Screens subjects for eligibility
• Coordinates participant medical tests and procedures.
• Collects data as required by the protocol
• Maintains study timelines.
• Maintains adequate inventory of study supplies
• Retains all study records in accordance with sponsor requirements, policies and procedures.
• Maintains effective and ongoing communication with sponsor, research participants and Principal Investigator during the course of the study.
• Assists Principal Investigator in preparation of any modifications to the scientific protocol in accordance with Federal regulations and sponsoring agency policies and procedures.

Required Experience, Skills and Abilities

• 1+ years of medical setting experience preferred
• Good leadership, problem solving and decision making skills are required.
• Demonstrated experience with Microsoft programs
• Strong critical thinking, teamwork and leadership skills
• Ability to function in a fast-paced and rapidly changing environment with openness to new ideas and the flexibility to adapt positively to changes in direction, priorities, schedules, or responsibilities
• Excellent time management skills with the ability to meet timelines
• Experience with the use of clinical databases or EMR systems
• Proficient in English with strong written and oral communication skills
• Proficient with Microsoft office suite (Excel, Word, Power Point)
• Valid Nursing License

Reach out to info@bwresearch.ca