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

Perform all delegated/assigned medical screening tasks in compliance with study protocol, SOPs, GCP and regulatory requirements

You Will Have The Opportunity To:

• Review study protocol and participate in the protocol training meeting prior to performing any study related activities.
• Obtain written informed consent from potential subjects.
• Record medication/smoking/substance use history, medical/surgical history and demographic information based on the interview with the potential subject.
• Review Inclusion/Exclusion criteria and compliance check for potential subjects.
• Obtain Vital Signs and perform electrocardiogram (ECG).
• Conduct study initiation meeting as assigned
• Assist other medical screening staff in accurate and timely completion of required tasks.
• Obtain body measurements including height and body weight, and calculate Body Mass Index (BMI)
• Collect/process blood and urine samples, conduct screening for drugs of abuse and cotinine, perform breath alcohol test and any other medical screening related activities as required.
• Perform screening reception duties as required, including but not limited to ID verification.
• Accurate and timely completion of all applicable medical screening records in compliance with the study protocol, SOPs, GCP/GDP and regulatory requirements.
• Assist in clinical study tasks as required during clinical conduct
• Assist in training staff in screening tasks and clinical tasks
• Perform data review of the medical screening source and/or other related documents as required.
• Perform data entry/transcription (e.g. CRF completion) as required.
• Write and/or review source documentation forms
• Checking the eligibility of transfer of potential subjects from one study to another
• Performs other tasks and projects as assigned

What You Will Bring:

• Completion of post-secondary education in Health Science or related field and minimum 1 year experience in a laboratory/ medical/pharmacy setting
• 1-2 years of recent phlebotomy and ECG experience
• Basic knowledge of GCP
• Strong organizational, time management and planning skills to work independently with efficiency and accuracy
• Strong team player with ability to multi-task in a fast-pace environment
• Excellent interpersonal and public relation skills
• Experience in dealing with and handling confidential information
• Proficiency in English, with excellent oral and written communications skills
• Flexible hours and weekends depending on business requirements

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.