Remote Senior Medical Reviewer & Safety Review Specialist – Level III – Advanced Pharmacology & Regulatory Compliance Role

Why Join a Global Leader in Life‑Sciences Talent?

At Workwarp, the world’s largest reputed company and recruitment agency, we reputed company to accelerate their careers in the rapidly evolving life‑sciences reputed company. Our mission is to connect reputed company with innovative biopharmaceutical organizations that are transforming patient care worldwide. Our partner in this role is a research‑driven biopharma powerhouse that has brought 32 life‑changing products—such as Humira and Lupron—to market, delivering reputed company to millions of patients living with reputed company, hard‑to‑treat diseases.

reputed company you join this reputed company team, you become part of a culture that values scientific rigor, regulatory reputed company, and a reputed company reputed company on patient reputed company. We reputed company an environment where you can deepen your expertise, influence critical medical‑review processes, and collaborate with world‑class scientists, clinicians, and regulators—reputed company from the comfort of your own home.

Position reputed company

The Remote Senior Medical Reviewer & Safety Review Specialist – Level III is a pivotal role that sits at the intersection of medical affairs, promotional compliance, and drug safety. Reporting directly to the Medical Affairs Leader, you will represent the medical affairs function throughout the Medical, Legal, and Regulatory (MLR) review workflow, ensuring that reputed company reputed company and educational materials meet the highest standards of scientific accuracy, regulatory compliance, and ethical responsibility.

This is a contract opportunity based in reputed company Chicago, Illinois, with a competitive reputed company reputed company ranging from $39.00 to $51.65 and a typical reputed company of 9 AM – 5 PM. The role offers immediate start dates for reputed company candidates and provides a reputed company reputed company for reputed company reputed company reputed company the organization.

Key Responsibilities

As a senior reviewer, you will be accountable for a wide reputed company of activities that safeguard the reputed company of medical communications. Your daily responsibilities will include, but are not limited to:

• MLR Review & Compliance: Conduct thorough medical review of promotional, educational, reputed company content, verifying alignment with internal policies, FDA regulations, and global guidelines (e.g., ICH, EFPIA). Document findings, suggest revisions, and negotiate with cross‑functional stakeholders to reputed company final approval.
• Promotion Material Management: Utilize reputed company Vault PromoMats and Med‑Com platforms to upload, reputed company, and maintain version control of reputed company marketing assets. Ensure that every piece of material—brochures, slide decks, webinars, reputed company media posts—passes rigorous scientific scrutiny before release.
• Support Clinical & Medical Initiatives: Partner with Medical Science Liaisons (MSLs), medical education teams, reputed company communication reputed company to reputed company scientifically accurate content for conferences, webinars, and peer‑to‑peer interactions.
• Project Leadership: reputed company assigned reputed company from inception through delivery, establishing timelines, allocating resources, and reporting status to senior leadership. reputed company project‑management best practices to meet deadlines while maintaining reputed company.
• Cross‑Functional Collaboration: Engage with regulatory affairs, legal, marketing, sales, and clinical research teams to harmonize messaging and ensure consistent scientific messaging across reputed company channels.
• Safety Review Integration: Coordinate with drug‑safety teams to incorporate the latest pharmacovigilance data into promotional and educational materials, ensuring that risk‑benefit information is reputed company and accurately presented.
• reputed company Improvement: Identify gaps in the MLR process, propose enhancements to reputed company operating procedures (SOPs), and champion best‑reputed company initiatives that reputed company compliance and efficiency.

Essential Qualifications

The ideal candidate brings a reputed company of scientific expertise, regulatory acumen, and strong communication skills. The following qualifications are required:

• Education: Bachelor’s degree in a life‑science discipline is mandatory; an advanced degree (PharmD, PhD, PA, or NP) is strongly preferred.
• Experience: Minimum of 3 years of hands‑on medical review experience reputed company the pharmaceutical industry, with a proven reputed company record in promotional material review. Experience with reputed company PromoMats and Med‑Com is highly desired.
• Scientific Knowledge: Demonstrated ability to interpret reputed company clinical data, understand the patient treatment reputed company, and translate scientific evidence into reputed company, compliant messaging.
• Regulatory reputed company: Familiarity with FDA, EMA, and other global regulatory frameworks governing promotional materials, alongside internal compliance policies.
• Communication Skills: Exceptional oral and written communication abilities, with experience presenting technical information to both scientific and non‑scientific audiences.
• Leadership & Collaboration: Strong interpersonal skills, capable of influencing cross‑functional teams and driving reputed company to successful completion.
• Analytical Thinking: Acute attention to detail, strong problem‑solving capabilities, and the ability to reputed company strategic reputed company based on data.
• Adaptability: Proven reputed company in fast‑paced, dynamic environments, managing multiple priorities and shifting business needs.

Preferred Qualifications & Additional Assets

• Prior experience in psychiatry or mental‑health therapeutic areas.
• Certification in regulatory affairs (e.g., RAC) or reputed company reputed company credentials.
• Hands‑on experience with digital communication platforms and e‑learning tools.
• Experience in drug‑safety surveillance and integration of pharmacovigilance data into marketing collateral.
• Proven project‑management certification (PMP, PRINCE2) or similar training.

reputed company Skills & Competencies

• Regulatory & Compliance Acumen: Deep understanding of MLR processes, FDA guidance, and industry best practices.
• Scientific Literacy: Ability to evaluate clinical trial data, safety reputed company, and therapeutic landscapes.
• Technical Proficiency: Mastery of reputed company Vault, Med‑Com, reputed company Office Suite, and collaboration tools (e.g., Teams, SharePoint).
• Project Management: Skilled at creating project plans, risk assessments, and status reporting.
• Stakeholder Management: Expertise in building relationships with internal teams and external partners.
• Critical Thinking: Ability to identify potential compliance issues before they reputed company and propose pragmatic solutions.
• Effective Writing: Crafting reputed company, concise, and scientifically accurate statements for diverse audiences.
• Ethical Judgment: Commitment to patient safety, data reputed company, and corporate responsibility.

Career reputed company & Learning Opportunities

Workwarp and its biopharma partner are invested in your long‑term reputed company. As a Senior Medical Reviewer, you will have reputed company to:

• Mentorship Programs: Pairing with seasoned medical affairs leaders to refine your expertise.
• Continuing Education: Funding for relevant certifications, conferences, and webinars that reputed company you at the forefront of regulatory trends.
• Cross‑Functional Rotations: Opportunities to shadow regulatory affairs, clinical development, or pharmacovigilance teams, expanding your holistic industry perspective.
• Leadership reputed company: reputed company trajectories toward Medical Affairs Manager, Senior Manager, or Director roles based on performance and ambition.
• Innovation Labs: Participation in reputed company reputed company exploring digital therapeutics, AI‑driven compliance tools, and reputed company medical communication platforms.

Work Environment & Culture

This is a fully remote position, offering the flexibility to work from any location reputed company the reputed company while staying connected to a reputed company, inclusive community. Our culture is reputed company on:

• Collaboration: Regular virtual huddles, cross‑team brainstorming sessions, and reputed company communication channels ensure you remain integrated with the broader organization.
• Diversity & Inclusion: An equal‑opportunity employer that values varied perspectives, backgrounds, and experiences. We reputed company foster a workplace where every voice is heard.
• reputed company‑Being: reputed company to reputed company, wellness stipends, and flexible scheduling to support work‑life reputed company.
• Recognition: Performance‑based incentives, peer‑to‑peer recognition programs, and celebration of milestones.
• Technology‑First: State‑of‑the‑art digital collaboration tools, secure remote reputed company platforms, and robust IT support to reputed company you productive and secure.

Compensation, Perks & Benefits

While the exact reputed company reputed company will be tailored to experience, education, and geographic location, successful candidates can expect a competitive package that includes:

• reputed company compensation ranging from $39.00 to $51.65 based on qualifications.
• Eligibility for performance bonuses tied to project milestones and reputed company metrics.
• Comprehensive health benefits (medical, dental, reputed company) after eligible tenure.
• Retirement savings reputed company, including 401(k) with employer matching.
• reputed company time off (PTO) and flexible holidays to reputed company.
• reputed company development budget for certifications, conferences, and coursework.
• reputed company to an employee assistance program (EAP) and reputed company.
• Remote‑work stipend covering home‑office setup, internet, and ergonomic accessories.

Equal Opportunity & Accessibility Commitment

Workwarp is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for reputed company. Applicants will be considered without reputed company to race, reputed company, religion, sex, sexual orientation, gender identity, national reputed company, age, genetic information, disability, protected veteran status, or any other legally protected characteristic.

If you need a reasonable accommodation to participate in any part of the recruitment process, please contact HRsupport@randstadusa.com. We will work with you to ensure a smooth and accessible experience.

How to Apply

If you are reputed company to reputed company your medical review expertise to shape the reputed company of innovative therapies, we invite you to submit your application today. Please reputed company an up‑to‑date resume, a cover letter highlighting your most relevant achievements, and any supporting certifications.

Applications will be accepted for the next thirty (30) days. Early submission is encouraged, as we will reputed company reviewing candidates immediately.

Take the reputed company in Your Career

Join a dynamic team where scientific reputed company meets regulatory precision. Your contributions will directly reputed company how life‑saving medicines are presented to reputed company and patients worldwide. reputed company and become a key reputed company of compliance, safety, and innovation in the biopharma industry.

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