Research Assistant

PPG US ProPharma Group, LLC; Windsor; Remote; CAD 45,000 - 65,000; Full time

Job summary

A healthcare consulting firm is seeking a Research Assistant to support remote site activities. This role involves managing site communications, performing data entry, and ensuring compliance with regulations. The ideal candidate will have a Bachelor’s degree and experience in research. Strong communication and critical thinking skills are essential. This position allows for independent and collaborative work in a supportive environment.

Benefits

Diversity and inclusion commitment

Supportive work environment

Qualifications

• Minimum of 1 year related experience in research.
• Experience with study team preferred.

Responsibilities

• Serve as primary contact for Site communications.
• Support pre-screening and data entry tasks.
• Maintain documentation for compliance.
• Assist with study-related activities.

Skills

Critical thinking

Strong communication skills

Technology management

Ability to work independently

Organization and multitasking

Education

Bachelor’s degree or equivalent experience

Job description

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle.With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.

The Research Assistant position is responsible for supporting remote site activities for assigned projects.

Essential Functions:

• Serve as point of contact for day-to-day Site communications, document submissions and activity coordination.
• Support pre-screening as assigned.
• Perform data-entry, evaluate and respond to system queries and monitor clinical databases as assigned.
• Establish and maintain timely Site communication as assigned.
• Maintain documentation which complies with IRB/FDA policies.
• Assist with study closeout.
• Assist site with other study-related activities as directed.
• Other duties as assigned.

Necessary Skills and Abilities:

• Ability to manage technology and web-based research platforms on PC (Microsoft OS) laptop in the remote workspace.
• Study Team experience is ideal.
• Critical thinking skills.
• Strong communication Skills (verbal and written).
• Ability to work independently, and collaboratively with other CSCs to delegate tasks as needed.
• Working location that has the ability to maintain privacy.
• Well organized and able to multitask.
• Able to work independently and as a team member.
• Able to take initiative while following directives.
• Professional, well spoken, articulate.

Educational Requirements:

• Bachelor’s degree or equivalent experience defined as a minimum of 1 year related, combined experience in education, knowledge and skills that will allow one to perform the tasks of the role proficiently.

ExperienceRequirements:

• Research experience preferred.

We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.

***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***

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