Consultant, Regulatory Sciences

at  ProPharma Group

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. As the world’s largest RCO (Research Consulting Organization), 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 RS Consultant is responsible for providing support to Project Managers, Scientific and/or Senior Staff as it relates to regulatory and scientific assignments.

Essentially Functions

• Retrieve, research, and compile data to support client projects.
• Conduct analysis of scientific data and regulatory information.
• Summary regulatory information and pertinent scientific literature for assigned projects.
• Ensure client ready work product, on time and within budget.
• Prepare populated templates for use by clients and/or internal project teams.
• Communicate directly with clients, at the discretion of project managers/leads.
• Support the strategic priorities and direction, as well as the day to day polices and practices, of the Company.
• Actively participate and contribute to job creation marketing efforts within the Company.
• Prepare and maintain Standard Operation Procedures (SOPs) for the research function .
• Collaborate with peers and colleagues to develop knowledge of information sources and retrieval techniques.
• Manage databases and regulatory communication logs.
• May act as project manager on smaller assignments.

Necessary Skills and Abilities

• Excellent research skills.
• Excellent verbal and written communication skills.
• Proficient in MS Office with the ability to operate within database applications.
• Detail-oriented, conscientious, and organized with the ability to multi-task and prioritize to manage deadlines.
• Proficient in the use of technology tools and terminology.

Educational Requirements

• Bachelor’s Degree in a life science or related field of study.

Experience Requirements

• 2+ years of regulatory or related experience.

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.

Please refer the Job description for details