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Remote Pharmaceutical Risk Management Jobs in Chicago, IL

Bcbsa

Director of Audit - Synergie (Remote)

Chicago, IL · Remote

$150K - $200K/yr

The Director of Audit is responsible for overseeing the organization's client and pharmaceutical ... Risk Management and Compliance. 35% * Collaborate with Finance, Legal, and IT to strengthen ...

CNA

Risk Control Consultant, Virtual Center

Chicago, IL · On-site +1

$72K - $141K/yr

Under general management direction, works within broad limits of authority requiring a high degree ... Performs remote workplace/work site risk evaluation and remote consultative risk improvement ...

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Remote Pharmaceutical Risk Management information

See Chicago, IL salary details

$23.2K

$121.8K

$216.3K

How much do remote pharmaceutical risk management jobs pay per year?

As of Jul 29, 2026, the average yearly pay for remote pharmaceutical risk management in Chicago, IL is $121,823.00, according to ZipRecruiter salary data. Most workers in this role earn between $87,000.00 and $149,400.00 per year, depending on experience, location, and employer.

What is remote pharmaceutical risk management?

Remote pharmaceutical risk management involves identifying, assessing, and mitigating risks associated with the development, manufacturing, and distribution of pharmaceutical products, all while working from a remote location. Professionals in this role use digital tools and communication platforms to monitor compliance, analyze data, and ensure that safety and regulatory standards are met. This approach allows for flexibility and can support global teams, but also requires strong digital collaboration and data security practices.

What are the key skills and qualifications needed to thrive as a Remote Pharmaceutical Risk Management professional, and why are they important?

To thrive in Remote Pharmaceutical Risk Management, you need a solid background in pharmacy, pharmacology, or related life sciences, often complemented by a relevant degree and experience in risk assessment or regulatory affairs. Familiarity with risk management plans (RMPs), pharmacovigilance databases, and regulatory compliance tools such as MedDRA and Argus Safety is typically required. Strong analytical thinking, attention to detail, and effective written and verbal communication are critical soft skills for this role. These competencies ensure accurate risk identification, regulatory compliance, and effective communication of safety information, which are vital for protecting patient safety and supporting regulatory approval.

What are some common challenges faced by professionals in remote pharmaceutical risk management roles, and how can they be addressed?

Professionals in remote pharmaceutical risk management often face challenges such as ensuring effective communication with cross-functional teams, maintaining data security, and staying current with regulatory requirements. Navigating time zone differences and building relationships virtually can also be difficult. To address these challenges, it's important to leverage secure collaboration tools, schedule regular check-ins, and prioritize continuous training on evolving regulations. Building strong digital communication habits and fostering a culture of transparency can further enhance remote teamwork and overall risk management effectiveness.
What are the most commonly searched types of Pharmaceutical Risk Management jobs in Chicago, IL? The most popular types of Pharmaceutical Risk Management jobs in Chicago, IL are:
What are popular job titles related to Remote Pharmaceutical Risk Management jobs in Chicago, IL? For Remote Pharmaceutical Risk Management jobs in Chicago, IL, the most frequently searched job titles are:
What job categories do people searching Remote Pharmaceutical Risk Management jobs in Chicago, IL look for? The top searched job categories for Remote Pharmaceutical Risk Management jobs in Chicago, IL are:
Remote Pharmaceutical Risk Management jobs near you
Clinical Product Surveillance Specialist

Clinical Product Surveillance Specialist

Medline

Northfield, IL • On-site, Remote

Full-time

Medical, Life, Retirement, PTO

Posted 17 days ago

Medline Industries rating

7.5

Company rating: 7.5 out of 10

Based on 249 frontline employees who took The Breakroom Quiz

261st of 536 rated manufacturers

Job description

Job Summary
Under general supervision, the Clinical Product Surveillance Specialist is responsible for independently using knowledge of clinical workflows and product use when investigating post-market complaints and providing clinical resource support to internal and external customers. This role acts as a patient safety advocate and participates in various cross-functional activities that include, but are not limited to Complaint Handling, Risk Management, Design Quality, and Regulatory Compliance, to support product safety and efficacy and recommend improvements and/or corrections as needed.
Job Description
Responsibilities:
  • Identify and investigate domestic and international post-market complaints with a potential safety issue and escalate complaints for further investigations as needed.
  • Ensure adverse event reports (i.e. MDRs, ICSRs) are processed, prepared, and submitted to the FDA within regulation timelines.
  • Process FDA reportable post-market complaints and assist in coordinating international adverse event reporting with local health authorities or authorized representatives.
  • Collaborate with team members and act as a clinical resource for internal and external customers.
  • Ensure communications are created and issued to internal and external customers. Review customer responses for technical and clinical accuracy as related to Medline products.
  • Provide clinical insight, evaluation, and resolution during post-market, risk management, and design development/modifications processes for new and existing Medline products.
  • Participate in the analysis of safety and risk data within areas of responsibility and identify actionable findings, trends, or product safety issues that require further investigations.
  • Assess clinical, health, and safety risks during Health Hazard Evaluations, product recall or field action determinations, and acceptance of product as-is.
  • Ensure compliance with applicable post-market regulations for areas of responsibility and participate in regulatory audits, regulatory body communications, and/or additional information requests as applicable.
  • Participate in process improvements and Corrective and Preventative Actions (CAPAs).
  • Participate in the development and maintenance of processes/procedures associated with Adverse Event Reporting, Risk Management, and Standard Operating Procedures (SOPs) associated with Clinical Risk Evaluation.
  • Facilitate clinical safety meetings and conduct trainings related to post-market surveillance, clinical use, product risk, and SOP requirements.
  • Maintain active Registered Nurse (RN) licensure and good standing with state or other governing licensure body.

Qualifications:
  • Bachelor's Degree in Nursing (BSN) with at least 5 years of patient care experience OR a BSN with 4 years or less of patient care experience and 2 years of experience in a similar role.
  • Actively licensed as an RN to administer healthcare and in good standing with state or other governing licensure body.

Knowledge / Skills / Abilities:
  • Knowledge of quality improvement and patient safety.
  • Understanding of clinical standards, processes, and workflows.
  • Familiarity with medical devices and pharmaceuticals related to patient safety.
  • Ability to assess clinical outcomes, analyze data, and present findings to various audiences.
  • Proficiency in Microsoft Office (Outlook, Teams, Excel, Word, PowerPoint).
  • Strong work ethic and proactive approach to responsibilities.
  • Customer-focused with a results-oriented mindset.
  • Ability to make sound judgments prioritizing patient safety.
  • Team player with analytical skills and a positive attitude.
  • Experience in data analysis and reporting to identify trends and solutions.
  • Experience working with cross-functional teams to solve complex problems.
  • Effective time management skills to handle multiple projects and deadlines.
  • Ability to work independently and escalate issues when necessary.
  • Problem-solving skills to overcome obstacles and find successful solutions.

Preferred Qualifications:
  • Advanced degree in nursing, medical or healthcare sciences, or other healthcare related field.

Certification / Licensure
  • Licensed, registered, or certified by a state or other governing body to administer health care. Certification in a nursing specialty (i.e. APRN, CNS, CEN, CCRN, WOCN, etc.) or other healthcare related field.

Work Experience
  • Experience within a Perioperative/OR, Critical Care (i.e. Emergency Department, ICU, Step-Down ICU, Cath Lab, etc.), or Wound Care/Management setting.
  • Experience in clinical, medical device, or pharmaceutical risk management and/or within the medical device or pharmaceutical industry.
  • Experience or working knowledge of government and industry standards and regulations for medical products (i.e. 21 CFR 803, 21 CFR 314, 21 USC 379aa, 21 CFR 7, ISO 13485, ISO 14971, etc.).

Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education & training, and tremendous potential with a growing worldwide organization.
The anticipated salary range for this position:
$79,000.00 - $119,000.00 Annual
The actual salary will vary based on applicant's location, education, experience, skills, and abilities. This role is bonus and/or incentive eligible. Medline will not pay less than the applicable minimum wage or salary threshold.
Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions, paid time off, as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp. For a more comprehensive list of our benefits please click here.
We're dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging page here.
Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.

What Medline Industries employees say

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About Medline

Sourced by ZipRecruiter

Medline Industries, LP is the leading nationwide supplier of medical, surgical and pharmaceutical products to hospitals, nursing homes, HME providers, surgery centers, physician offices and home care/hospice settings.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Winnetka, IL, US

Year founded

1966

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