Overview Are you an accomplished Board Certified Orthopedic Surgeon physician? Are you passionate about your work/life balance? We are seeking flexible and experienced physicians for our medical reviewstream division. This telecommute role provides the ability for you to customize your schedule and caseload within a Monday - Friday work week and within business hours. Create a flexible work schedule and be compensated on a per case basis as a 1099 independent contractor. Candidates must have a CA license. JOB SUMMARY: Relying on clinical background, reviews health claims providing medical interpretation and decisions about the appropriateness of services provided by other healthcare professionals in compliance with Concentra Physician Review policies, procedures, and performance standards and URAAC guidelines and state regulations Responsibilities MAJOR DUTIES AND RESPONSIBILITIES: • Reviews medical files and provides recommendations for utilization review, chart reviews, medical necessity, appropriateness of care and return to work, short and long-term disability, Family and Medical Leave Act (FMLA), Group health and workers’ compensation claims. • Meets (when required) with Concentra Physician Review Medical Director to discuss quality of care and credentialing and state licensure issues.• Maintain proper credentialing and state licenses and any special certifications or requirements necessary to perform the job.• Returns cases in a timely manner with clear concise and complete rationales and documented criteria. • Telephonically contacts providers and interacts with other health professionals in a professional manner. Discusses the appropriate disclaimers and appeal process with the providers.• Attends orientation and training• Performs other duties as assigned including identifying and responding to quality assurance issues, complaints, regulatory issues, depositions, court appearances, or audits.• Identifies, critiques, and utilizes current criteria and resources such as national, state, and professional association guidelines and peer reviewed literature that support sound and objective decision making and rationales in reviews.• Provides copies of any criteria utilized in a review to a requesting provider in a timely manner Qualifications EDUCATION/CREDENTIALS: -Board certified MD, DO, with an excellent understanding of network services and managed care, appropriate utilization of services and credentialing, quality assurance and the development of policies that support these services. -Current, unrestricted clinical license(s) (or if the license is restricted, the organization has a process to ensure job functions do not violate the restrictions imposed by the State Board); -Board certification by American Board of Medical specialties or American Board of Osteopathic Specialties is required for MD or DO reviewer. -Must be in active medical practice to perform appeals JOB-RELATED EXPERIENCE:Post-graduate experience in direct patient careJOB-RELATED SKILLS/COMPETENCIES: -Demonstrated computer skills, telephonic skills-Demonstrated ability to perform review services.-Ability to work with various professionals including members of regulatory agencies, carriers, employers, nurses and health care professionals. -Medical direction shall also be provided consistent with the requirement that the physician advisor shall not have a financial conflict of interest -Must present evidence of current error and omissions liability coverage for job duties and activities performed-Managed care orientation-Knowledge of current practice standards in specialty-Good negotiation and communication skillsWORKING CONDITIONS/PHYSICAL DEMANDS: -Phone accessability -Access to a computer to complete reviews-Ability to complete cases accompanied by a typed report in specified time frames-Telephonic conferences This job requires access to confidential and sensitive information, requiring ongoing discretion and secure information management. Concentra is an Equal Opportunity Employer M/F/Disability/Veteran Concentra's Data Protection Commitment* Concentra is committed to protect patient data and to ensure privacy of personal and medical information.* Every Concentra colleague has the responsibility to adhere to data protection principles.* If a colleague's role includes handling or processing sensitive data, role-specific policies and requirements apply to ensure the protection of patient information.

Overview Are you an accomplished Board Certified Ophthalmologist? Are you passionate about your work/life balance? We are seeking flexible and experienced physicians for our medical reviewstream division. This telecommute role provides the ability for you to customize your schedule and caseload within a Monday - Friday work week and within business hours. Create a flexible work schedule and be compensated on a per case basis as a 1099 independent contractor. Candidates must have a Louisiana license. JOB SUMMARY: Relying on clinical background, reviews health claims providing medical interpretation and decisions about the appropriateness of services provided by other healthcare professionals in compliance with Concentra Physician Review policies, procedures, and performance standards and URAAC guidelines and state regulations Responsibilities MAJOR DUTIES AND RESPONSIBILITIES: • Reviews medical files and provides recommendations for utilization review, chart reviews, medical necessity, appropriateness of care and return to work, short and long-term disability, Family and Medical Leave Act (FMLA), Group health and workers’ compensation claims. • Meets (when required) with Concentra Physician Review Medical Director to discuss quality of care and credentialing and state licensure issues.• Maintain proper credentialing and state licenses and any special certifications or requirements necessary to perform the job.• Returns cases in a timely manner with clear concise and complete rationales and documented criteria. • Telephonically contacts providers and interacts with other health professionals in a professional manner. Discusses the appropriate disclaimers and appeal process with the providers.• Attends orientation and training• Performs other duties as assigned including identifying and responding to quality assurance issues, complaints, regulatory issues, depositions, court appearances, or audits.• Identifies, critiques, and utilizes current criteria and resources such as national, state, and professional association guidelines and peer reviewed literature that support sound and objective decision making and rationales in reviews.• Provides copies of any criteria utilized in a review to a requesting provider in a timely manner Qualifications EDUCATION/CREDENTIALS: -Board certified MD, DO, with an excellent understanding of network services and managed care, appropriate utilization of services and credentialing, quality assurance and the development of policies that support these services. -Current, unrestricted clinical license(s) (or if the license is restricted, the organization has a process to ensure job functions do not violate the restrictions imposed by the State Board); -Board certification by American Board of Medical specialties or American Board of Osteopathic Specialties is required for MD or DO reviewer. -Must be in active medical practice to perform appeals JOB-RELATED EXPERIENCE:Post-graduate experience in direct patient careJOB-RELATED SKILLS/COMPETENCIES: -Demonstrated computer skills, telephonic skills-Demonstrated ability to perform review services.-Ability to work with various professionals including members of regulatory agencies, carriers, employers, nurses and health care professionals. -Medical direction shall also be provided consistent with the requirement that the physician advisor shall not have a financial conflict of interest -Must present evidence of current error and omissions liability coverage for job duties and activities performed-Managed care orientation-Knowledge of current practice standards in specialty-Good negotiation and communication skillsWORKING CONDITIONS/PHYSICAL DEMANDS: -Phone accessability -Access to a computer to complete reviews-Ability to complete cases accompanied by a typed report in specified time frames-Telephonic conferences This job requires access to confidential and sensitive information, requiring ongoing discretion and secure information management. Concentra is an Equal Opportunity Employer M/F/Disability/Veteran Concentra's Data Protection Commitment* Concentra is committed to protect patient data and to ensure privacy of personal and medical information.* Every Concentra colleague has the responsibility to adhere to data protection principles.* If a colleague's role includes handling or processing sensitive data, role-specific policies and requirements apply to ensure the protection of patient information.

Protecting our tomorrow Job Title: Head of Medical Affairs & GCSP (Global Clinical Safety & Pharmacovigilance) Location: Remote – US East Coast Department: Research & Development Reports To: Senior VP of R&D Salary Range: $325k - $415k About Bavarian Nordic At Bavarian Nordic, we are dedicated to protecting lives and advancing global health through innovative vaccines. As a global leader in smallpox and mpox vaccines, our growing portfolio includes market-leading vaccines against rabies, chikungunya, cholera, and typhoid. Our mission is simple: to improve quality of life worldwide by preventing infectious diseases. We are headquartered in Denmark and have offices across Europe and North America. Position Overview We’re looking for an experienced Head of Medical Affairs & GCSP (Global Clinical Safety and Pharmacovigilance) providing medical leadership across GCSP, Epidemiology, Medical Affairs, and Medical & Process Compliance. You will guide patient safety and benefit–risk, shape evidence generation and medical governance, and partner closely with Regulatory, Clinical Development, Quality, CMC/Manufacturing, Commercial, and Market Access to ensure scientific rigor and aligned execution across the product lifecycle. The position reports to the SVP of R&D and should be based on the East Coast of the United States - global travel up to ~30% should be expected. Key Responsibilities - ·Lead and develop high-performing GCSP, Epidemiology, Medical Affairs, and Medical & Process Compliance teams, including people leadership, budgets, and talent development - ·Have oversight of the GCSP team and QPPV office - ·Set and execute global Medical Affairs strategy aligned to development milestones, regulatory interactions, and commercialization plans; ensure medical accuracy and balance across all external scientific content - ·Establish and scale regional medical networks to support local commercial teams, capture insights, and localize global strategies - ·Own medical information capabilities and responses to unsolicited medical inquiries - ·Drive late-stage and post-approval evidence generation, including RWE, observational, and epidemiological studies - ·Institute robust medical governance appropriate for company growth; chair and/or contribute to internal medical governance committees - ·Partner deeply with Clinical Development to inform future trials and label expansions; collaborate across Regulatory, Manufacturing/CMC, Quality, Commercial, and Market Access - ·Build strategic external relationships with key opinion leaders and public-health stakeholders Qualifications - Advanced degree is required, and an MD qualification is preferred for this role - Expertise in medical affairs, clinical safety, and global pharmacovigilance, with a strong foundation in immunology, epidemiology, and vaccine safety - 10+ years’ experience in a similar role - Strategic mindset and operational rigor to ensure patient safety and scientific excellence across the product lifecycle - 10+ years’ experience from a leadership role with both direct and indirect reports - Exceptional communicator who can translate complex medical and regulatory topics into clear, actionable guidance for both scientific and non-scientific stakeholders - As a trusted advisor to senior leadership, you provide confident counsel on medical strategy, compliance, and risk management - As a leader, you’re hands-on and people-focused—ready to coach, mentor, and elevate high-performing teams across regions—while orchestrating medical governance, evidence generation, and external collaborations with precision and credibility - Curious and data-driven; you monitor emerging trends, synthesize real-world evidence, and challenge assumptions to inform better decisions - Most importantly, you thrive in change; your judgment, integrity, and resilience help safeguard patient safety and support our transition from development to full commercialization in a fast-moving, life-science environment Why Join Us Join a passionate, mission-driven global biotech committed to protecting lives. At Bavarian Nordic, you’ll find a collaborative culture, flexible work environment, and opportunities for ongoing professional development and growth. Bavarian Nordic is a global vaccine company with a mission to improve health and save lives through innovative vaccines. We are a preferred supplier of mpox and smallpox vaccines to governments to enhance public health preparedness and have a leading portfolio of travel vaccines. We are headquartered in Denmark and have manufacturing, research, and sales offices across Europe and North America. Bavarian Nordic is an Equal Opportunity Employer. All qualified applications will receive consideration for employment and will not be discriminated against based on race, color, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. For more information, visit www.bavarian-nordic.com #LI-MA1

Role Description The Pharmacovigilance Physician will report to the VP of Pharmacovigilance. The PV/Drug Safety physician will be a medical professional responsible for ensuring drug safety throughout a product's lifecycle by detecting, assessing, and managing adverse events. They will conduct medical reviews of safety reports (ICSRs), identify risks, and ensure compliance with global regulations. You will be responsible for: - Providing clinical and scientific leadership within the pharmacovigilance function. - Engaging cross-functional internal workstreams including therapeutic area development, biostatistics, clinical operations, and regulatory affairs. - Providing clinical input to the design of clinical trials, signal detection and management activities, post-authorization studies, risk minimization, and risk communication. - Performing case series analysis of adverse events and review of passive surveillance data mining signals of disproportionate reporting as well as safety issues from other sources. - Leading clinical safety and benefit-risk sections of regulatory documents and preparation for meetings with regulatory and public health authorities as well as advisory committees. - Performing post-marketing surveillance and regulatory reporting, as needed. - Guiding the operations of contract research organizations. - Serving as an exemplary leader, mentor, and trainer. Qualifications - MD, D.O. or non-US equivalent required. - Residency training & board certification highly preferred. - Clinical practice experience highly preferred. - Experience working with public health agencies highly preferred. - 2-4 years of prior experience in pharmacovigilance in an industry setting, either in a comparable role, or in clinical development. Requirements - Proven ability to collaborate effectively within dynamic and fast-moving technical teams to deliver high-quality results within established timelines. - Utilize technology supporting pharmacovigilance (e.g. for signal detection and regulatory reporting). - Interpret and integrate concepts and guidelines from FDA, EMA, PMDA and other regulatory agencies, government research organizations (e.g. NIH), public health agencies and nongovernmental organizations, and clinical practice groups. - Investigate new safety issues. - Communicate medical product benefits and risks to regulatory and public health authorities as well as the public. - Ability to thrive in a fast-paced environment while providing appropriate attention to detail. - Excellent analytical, problem-solving, strategic planning, and interpersonal skills. Behavioral skills to be successful... - Problem-Solver: As an action-oriented self-starter, you’re eager to apply your expertise in diagnosing inefficiencies, determining root causes, and recommending solutions to complex challenges. - Personable: You establish and nurture highly effective relationships with colleagues and key stakeholders that support and advance project goals and objectives. - Credible: With a thorough understanding of clinical methodologies and providing sound analytical support, you quickly establish credibility as a reliable resource. - Emotional intelligence: Curiosity, and a knack to figure out a way to build something better. - Communication: Effectively listens, conveys, and receives ideas. Maintains a consistent flow of information. A strong presenter and effective communicator with the ability to influence stakeholders. - Accountability: Acts with a clear sense of ownership - whether the task is in their role description. Holds yourself and others accountable to execute all tasks at hand through seen and unforeseen circumstances with high quality and integrity. - Adaptability: Can manage in an environment of ambiguity. Embraces the change of a new system, process, technology, or idea in the organization. You could reassess priorities, alter goals and take risks. Benefits - Competitive Base Salary, Bonus, and Equity Plans. - Unlimited Vacation and 10 Sick Days Annually. - Excellent Medical, Dental, and Vision Coverage. - 401K with Company Matching. - And much more!