Clinical Research Manager - Montréal, Canada - Noze

Noze

Verified Company

Montréal, Canada

2 weeks ago

Posted by:

Sophia Lee

beBee Recruiter

Description

Who We Are
Noze has digitized the sense of smell. We've done for the nose what the camera did for the eyes and the microphone did for the ears. It took six years and some help from NASA but we did it. Now it's time for us to bring it to the world.

Are you interested in rolling up your sleeves and building our marketing engine from the ground up? In this role, you will build, own and drive the marketing function while working across departments to collaborate on new initiatives.

Reporting directly to the Chief Executive Officer, you will take the lead on all things marketing to drive awareness and build our partnership pipeline.

People who succeed at Noze have a sense of urgency, a ton of initiative, infinite curiosity, strong internal drive, and an enthusiasm for technology.

If you're bursting with fresh ideas and want to join a company in its journey to change the status quo, then this opportunity is for you

Who You Are

What You Will Do

Identify and research potential clinical research partners, including investigators, research hospitals, medical centers, and contract research organizations (CROs).
Conduct discovery and evaluate the feasibility of potential clinical partners, and develop proposals outlining the potential collaboration opportunities and benefits.
Develop and maintain strong partnerships with new clinical research partners to facilitate the recruitment and enrollment of patients for clinical trials.
Collaborate with new clinical research partners to develop clinical trial protocols, manage associated budgets and ensure compliance with regulatory guidelines.
Manage and oversee the clinical research project lifecycle, including study startup activities, monitoring, and closeout.
Ensure that all clinical trials are conducted in accordance with Good Clinical Practice (GCP) guidelines, applicable regulations, and internal standard operating procedures (SOPs).
Lead the informed consent process including interactions with the IRB and discussions with research participants, including answering any questions related to the study.
Train clinical teams on some specific procedures related to the individual studies (such as the use of a new technology for data collection) that will yield high data quality and integrity.
Monitor and track the progress of clinical trials. Provide regular updates to senior management and knowledge share with key stakeholders / team members within the organization.
Manage and resolve any issues that arise during the clinical trial process, including protocol deviations and adverse events.
Provide support and training to new clinical research partners on study procedures, protocol requirements, and data management.
Prepare other study materials as requested by the PI. These study materials include, but are not limited to protocol, informed consent documents, case report forms (CRFs), enrollment logs, and SOPs.
Ensure that all clinical trial documentation is accurate, complete, and submitted in a timely manner.
Maintain knowledge of industry trends and best practices in clinical trial management and compliance.

What You Need

Advanced degree (e.g., Master degree, MD, PhD) in Biomedical sciences, Pharmacy, Pharmacology, RN or an equivalent combination of education, training and experience.
5 plus years of managerial experience in leading clinical projects and partnerships using medical device technologies
Strong knowledge of clinical trial regulations, guidelines, and best practices.
Excellent interpersonal and communication skills with the ability to build strong. relationships with clinical partners and internal stakeholders.
Proven ability to manage multiple clinical trials simultaneously and meet timelines.
Strong problemsolving and analytical skills with attention to detail.
Ability to work independently and as part of a team in a fastpaced environment.
Experience with clinical trial software and electronic data capture (EDC) systems is a plus.
Certification in clinical research (CCRP, CCRC, or similar) is a plus.

What We Offer

The opportunity to join a forwardthinking company surrounded by a collaborative team of innovative thinkers;
A rewarding career path with diverse opportunities for professional growth;
A competitive compensation and benefits package including employer paid health and dental benefits for eligible employees;
A generous learning and development budget to attend conferences, classes and other professional development events;
A bunch of other perks that involve food, fun and travel.