Regulatory Affairs Coordinator Salary in Minneapolis, Minnesota

Recruiter: Spencer Gregory Hale Principal Reg Affairs Specialist About the role: At Boston Scientific, you'll discover a place where you can have meaningful purpose, improving lives through your life's work. In Rhythm Management (RM) we offer solutions for treating irregular heart rhythms and heart failure and protecting against sudden cardiac arrest. We continue to innovate in key areas and extending our products into new geographies and high-growth adjacency markets. This role will be responsible for working on Boston Scientific's novel Atrial Fibrillation technology, the FARAPULSE Pulsed Field Ablation (PFA) System. The FARAPULSE PFA System was the first PFA technology that received a CE Mark in Europe and recently received PMA approval in the US. PFA technology has the potential to alter the future of ablation therapy on a global scale as we expand the reach of this product into other geographies and with different indications. Under minimal supervision, the Principal Regulatory Af

Intern Job Description: Healthcare Industry Outreach and Compliance Research Position Overview: We are a start-up seeking motivated and detail-oriented interns to assist with outreach to healthcare companies and staffing agencies. The primary focus of this role will be to gather information on compliance rules and credentialing requirements for employees within the healthcare sector. This internship offers an excellent opportunity to gain hands-on experience in healthcare administration, compliance research, and professional communication within the industry, as well as future full-time employment as we grow. Key Responsibilities: Outreach and Communication: Conduct outreach to healthcare companies and staffing agencies via email, phone calls, and other communication channels. Clearly and professionally communicate the purpose of the research project and request information on compliance rules and credentialing requirements. Research and Data Collection: Utilize various resources to ga

Head, Corporate & Legal Affairs Strategic Advisor Reporting to CEO; Innovative CRO Remote Retained Search Summary: Cornerstone Search Group has been retained by a rapidly growing Clinical Research Organization funded by a thriving multi-billion-dollar parent Health Care Company. The Head of Corporate & Legal Affairs will report directly to the CEO, with whom Cornerstone has had over a decade-long relationship and is a well-respected, collaborative leader with a rich history of working for start-ups and well-established CROs. The Head of Corporate & Legal Affairs will provide expert organizational/corporate leadership guidance, seamlessly integrating legal compliance, risk management, and strategic decision-making as the business scales. Our client seeks an individual with a legal background, a business mindset, and a deep understanding of the life sciences, finance, and operations. They will be a trusted strategic partner collaborating closely with the CEO and must possess a true roll

Recruiter: Spencer Gregory Hale Regulatory Affairs Manager - Core CRM Sustaining Program Regulatory POC Team Purpose: The Rhythm Management (RM) Regulatory Affairs leadership team is a strategic partner that delivers innovative, efficient, and sustainable business and regulatory solutions for customers throughout the product lifecycle. This role is considered part of the RM RA Leadership team. This role will manage and provide leadership to 3-4 regulatory submission specialists. The Manager I for Cardiac Rhythm Management (CRM) would report to the CRM Director. The role is Hybrid, with office location in Arden Hills, MN. This role will be singularly focused on providing valued regulatory management support for high priority activity within the Core CRM Sustaining Program. This role will be expected to represent the Regulatory Affairs function during multiple cross-functional project meetings and fulfill a people management role with 3-4 Regulatory Affairs submission specialists as dire

Program Lead - Permanent - Remote Proclinical is seeking a Program Lead, Neurology to join a global biopharmaceutical company. This is a permanent role with the opportunity to work remotely. Primary Responsibilities In this role, you will spearhead and oversee the planning, execution and evaluation of scientific programs from preclinical through translational stages. Skills & Requirements: MS/PharmD/PhD in Chemistry, Biology, Biochemistry, business, or related healthcare area Preferred: PMP or CAPM or similar project management certification or equivalent experience Work experience: minimum of 7 years Prefer experience within preclinical stage *ophthalmic, otic, and/or neurology Working knowledge of relevant therapeutic areas and experience working within development of preclinical through translational stage clinical studies Sound knowledge of drug development and understanding of FDA and ICH GCP guidelines Proven problem solving and project management skills Excellent verbal and writ

Director of Policy & Regulatory Affairs | Eastern US, REMOTE |$165k - $175k base + bonus Are you a regulatory affairs and energy policy professional with experience in the RTOs (PJM), FERC and State Commissions? Are you looking for an opportunity to join a small, well-backed, company on the cutting edge of the clean energy transition? Do you enjoy keeping tabs on potential energy policy changes? If yes, please read on! The Senior Manager/Director of Policy and Regulatory Affairs will play a pivotal role in shaping and advancing our client's strategic initiatives across PJM and regulatory landscapes. You'll lead the charge in cultivating strong relationships, driving impactful policy positions, and navigating the dynamic arenas of federal and state regulatory agencies, as well as legislative bodies. In this role, you'll be at the forefront of crafting and championing policy stances in key PJM states, spearheading the development of state filings, and closely monitoring the ever-evolving