Study Prep Associate - Toronto, Canada - BioPharma Services Inc.

BioPharma Services Inc.

Verified Company

Toronto, Canada

3 weeks ago

Posted by:

Sophia Lee

beBee Recruiter

Description

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 startup spirit

The Role

Responsible for the preparation of all study related documents to ensure the quality, reliability, accuracy, completeness and consistency according to Protocol, SOPs and regulatory requirements.

Other responsibilities as assigned.

You Will Have The Opportunity To:

Responsible for the accurate and timely preparation and maintenance of all study related source documents, including creation of study specific forms in paper and electronic format
Ensures the accuracy, timely and organized completion of assigned tasks within the Clinic in adherence to and compliance with the study protocol, SOPs, GCP and all regulatory requirements
Responsible for the creation and maintenance of Sponsor requested source documents
Maintains accurate, complete, legible and timely records
Participates in the development of internal staff training programs
Assists with the preparation and maintenance of Clinic related documents for the Regulatory Binder
Ensures the maintenance of Bio Centre/Administration fax, printer and photocopy equipment
Performs other tasks as assigned and as training and experience allow

What You Will Bring:

College diploma in science or business administration preferred but not required
Excellent computer skills (e.g. MS excel, word, etc)
Excellent organizational skills with attention to details
Proven track record of attendance
Knowledge of ICH-GCPs and professional experience working in CRO preferred
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._