Job Description

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The Company

BioPharma Services Inc. is a subsidiary of Think Research.

BioPharma Services was founded by two surgeons dedicated to advancing medical science to improve the life and spirit of their patients. With this same dedication and vision in mind, these physicians brought life to BioPharma.

Through each success, and even some failures, the perpetual drive to make BioPharma great has been determined by the will and dedication of our people. The will to empower their colleagues, friends and teammates to excel in all facets of clinical research and inspire performance to achieve greatness.

It is with this same culture and brand of excellence that we welcome our clients. To experience the team community that has propelled us into a global leader in medical research, to be a client-focused partner, where people and patients matter.

Again, we invite you to come and meet our people. Our people who have learned that success is better achieved and celebrated as a team than as an individual.

Why Us?

• It's not every day that you have the chance to change the way your friends and family are cared for - Make an impact!
• Everything we do - and we do it with passion - is to improve the quality of life for patients who benefit from the clinical trials that we perform for global pharmaceutical companies.
• We're growing, and so will you with leaders who will support your development through mentorship and other opportunities

• Collaborative, creative, dynamic and flexible work environment, with a start-up spirit

The Role

The Nurse Manager is responsible for providing leadership, guidance, support and

training to the clinical (Safety Team) members, and to coordinate operational

activities of research studies within the department. The Nurse Manager leads and

directly supervises a team of clinical staff, such as RNs, RPNs, and

Medical Assistants, and is responsible for the team's clinical related activities, and

performance. The Nurse Manager will report to the Director, Clinical Operations, and

will provide insight and assistance with internal department budgets, planning, and

other clinical/administrative activities as required. The Nurse Manager will also work in

consultation with the Chief Medical Officer to assist with and manage clinical oversight.

You Will Have The Opportunity To:

• Ensure the general clinical duties are performed to prepare for the clinical study and proper monitoring of clinical activities.
• Oversees the execution of clinical trials; coordinating all study clinic activities to ensure all clinic needs are met (tasks, subject safety, work schedules, breaks, clinic set-up, etc.)
• Work collectively with the Director, Clinical Operations, Chief Medical Officer, and Manager, Clinical Operations as required.
• Analyze and develop action plans to address issues with study monitors, sponsors, and regulatory agencies.
• Organize, oversee, and conduct Safety Team staff training, performance reviews and coaching.
• Work with the Director, Clinical Operations to assist in evaluating HR requirements within the department.
• Ensure clinical trial activities are conducted in accordance with the Protocol, SOP, ICH, GCP and applicable regulatory requirements.
• Ensures the accuracy of the generated data in accordance with protocols, SOP, ICH, GCP and applicable regulatory agencies.
• Write, Revise, and approve SOP's and internal procedures.
• Participates in protocol review and development.
• Participates in project scheduling, assessing and establishing project milestones
• Review and/or approve the Safety Team staff schedule and task assignments.
• Assist Director, Clinical Operations and the Chief Medical Officer with day-to-day activities.
• Lead, train and coach the team to ensure proper planning, organization and execution of clinical research studies.
• Participates in strategic decisions and partnering activities to increase productivity, reduce costs, and ensure that corporate clinical goals are met on time and on budget.
• Participates on Safety Committee, Protocol Review Committee, Inter-departmental meetings as required.
• Actively analyze and develop action plans to address issues brought up by
• QA, QC, Study Monitors, sponsors and regulatory agencies.

What You Will Bring:

• RN, Nurse in good standing with appropriate college or regulatory body
• At least 5 years' experience in clinical research or related field
• Knowledge of good Clinical Practice
• Updated CPR and ACLS Certification
• Able to work in a research setting and aware of the confidentiality that is
• required in research
• Relevant previous management experience required

Think Research and all subsidiaries are proud to be an equal opportunity employer and is committed to creating a diverse and inclusive workplace, free of discrimination and harassment.

We provide equal employment opportunities (EEO) to all employees and applicants regardless of race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.

We are committed to providing accommodations for people with disabilities. Should you require an accommodation, we would like to work with you to meet your needs.