2

Overnight Remote Medical Reviewer Jobs in Puerto Rico

... Medical Affairs, IT, and HR. Key Responsibilities APAC Privacy Legal Advisor. Serve as the subject ... Advise on applicable transfer mechanisms and review/negotiate DPAs, vendor contracts, and data ...

Showing results 21-22

Overnight Remote Medical Reviewer information

What is an overnight remote medical reviewer?

Overnight Remote Medical Reviewers are healthcare professionals who assess medical records, insurance claims, or clinical documentation during nighttime hours while working remotely. Their primary responsibility is to ensure that the information complies with legal, regulatory, and organizational standards. They may review patient cases for medical necessity, accuracy, and completeness, and often provide recommendations or decisions to support insurance claims or healthcare providers. Working remotely allows them to serve organizations across different time zones, ensuring 24/7 coverage of medical review processes.

What are the key skills and qualifications needed to thrive as an overnight remote medical reviewer?

To thrive as an Overnight Remote Medical Reviewer, you need a clinical background (such as RN, MD, or PharmD), strong analytical skills, and experience with medical documentation and terminology. Familiarity with electronic health records (EHRs), medical coding systems like ICD-10, and secure remote review platforms is typically required. Excellent written communication, attention to detail, and self-motivation are important soft skills for working independently and ensuring accuracy. These skills ensure timely, accurate medical reviews that support patient care and compliance in a remote, overnight setting.

What are some common challenges faced by overnight remote medical reviewers, and how can they be managed?

Overnight Remote Medical Reviewers often face challenges such as working across different time zones, maintaining alertness during non-traditional hours, and handling complex cases with limited immediate supervision. To manage these challenges, it's important to establish a consistent sleep schedule, create a distraction-free workspace, and leverage digital communication tools to stay connected with colleagues and supervisors. Regularly participating in virtual team meetings and ongoing training also helps reviewers stay updated on protocols and maintain a sense of teamwork despite remote and overnight conditions.

What is the difference between Overnight Remote Medical Reviewer vs Telemedicine Physician?

AspectOvernight Remote Medical ReviewerTelemedicine Physician
CredentialsMedical license, board certification in relevant specialtyMedical license, board certification, often in primary care or specialty
Work EnvironmentRemote, reviewing claims and medical records overnightRemote or in-clinic, providing patient consultations via telehealth
Employer & IndustryInsurance companies, third-party administratorsHealthcare providers, telehealth platforms
Common Search/ComparisonYesNo

The Overnight Remote Medical Reviewer primarily evaluates medical records and claims overnight for insurance companies, requiring specialized credentials. In contrast, a Telemedicine Physician provides direct patient care remotely, often during regular hours. While both roles are remote healthcare positions, their responsibilities and work environments differ significantly.

What job categories do people searching Overnight Remote Medical Reviewer jobs in Puerto Rico look for?

The top searched job categories for Overnight Remote Medical Reviewer jobs in Puerto Rico are:

What cities in Puerto Rico are hiring for Overnight Remote Medical Reviewer jobs?

Cities in Puerto Rico with the most Overnight Remote Medical Reviewer job openings:

Regional Privacy Counsel - APAC

Bristol-Myers Squibb

On-site, Remote

Full-time

Posted 23 days ago


Bristol Myers Squibb rating

8.2

Company rating: 8.2 out of 10

Based on 51 frontline employees who took The Breakroom Quiz

33rd of 86 rated pharmaceutical


Job description

Working with Us Challenging. Meaningful. Life-changing.

Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.

From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us

Position Summary Bristol Myers Squibb is seeking an experienced and strategic Regional Privacy Counsel for the Asia-Pacific (APAC) region to join our Global Privacy Law & Compliance team. This role is critical in ensuring BMS' data privacy and protection practices comply with the diverse and evolving regulatory landscape across APAC jurisdictions, while enabling the business to innovate and operate efficiently. The Regional Privacy Counsel will serve as the primary legal advisor on all privacy matters affecting BMS' APAC operations, working cross-functionally with business units including Commercial, Medical Affairs, IT, and HR.

Key Responsibilities APAC Privacy Legal Advisor. Serve as the subject matter expert on data privacy laws across APAC jurisdictions, including China (PIPL, CSL, DSL), Japan (APPI), South Korea (PIPA), India (DPDPA), Singapore (PDPA), Australia (Privacy Act/APPs), New Zealand (Privacy Act 2020), Hong Kong (PDPO), and Southeast Asia (Thailand, Philippines, Malaysia, Indonesia, Vietnam, Taiwan, etc.) Business Stakeholder Advisory. Advise business partners on privacy risks and legal obligations associated with new and existing initiatives across the region

Compliance Program Advice. Work with Director, Global Privacy Compliance to ensure accurate and actionable regional privacy compliance program in alignment with global privacy standards and policies. Privacy Impact Assessments.

Conduct PIAs and DPIAs for APAC-specific initiatives and maintain records of processing activities (RoPA) for APAC entities. Regulatory Monitoring. Track regulatory developments across APAC and ensure timely updates to internal policies, procedures, and controls.

Cross-Border Data Transfers. Advise on applicable transfer mechanisms and review/negotiate DPAs, vendor contracts, and data sharing arrangements with APAC partners. Training & Awareness.

Develop and deliver region-specific privacy training programs for APAC employees, contractors, and third parties; foster a culture of privacy accountability. Incident Response. Support, as needed, APAC privacy incident triage, investigation, notification, and remediation efforts in coordination with IT department along.

Qualifications Education: Law degree (LLB, JD, or equivalent); license to practice law in at least one APAC jurisdiction. Experience: Minimum 7-10 years of legal experience, with at least 5 years focused on data privacy and protection law in the APAC region. Deep expertise in at least three or more APAC data privacy regimes (e.g., PIPL, APPI, PIPA, PDPA, DPDPA)

Demonstrated experience advising on cross-border data transfer mechanisms and international privacy frameworks. Prior experience in the life sciences, pharmaceutical, or healthcare sector strongly preferred. Proven ability to navigate complex, multi-jurisdictional privacy issues with business pragmatism.

Strong negotiation skills for data processing and vendor agreements. Excellent communication skills in English; proficiency in at least one additional APAC language (Mandarin, Japanese, or Korean) highly desirable. If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway.

You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as "Transforming patients' lives through science ", every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility.

Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

Supporting People with Disabilities BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com

Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement. Candidate Rights BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/ Data Protection We will never request payments, financial information, or social security numbers during our application or recruitment process

Learn more about protecting yourself at https://careers.bms.com/fraud-protection. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com

Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.

R1605226 : Regional Privacy Counsel - APAC


What Bristol Myers Squibb employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


Bristol-Myers Squibb logo

About Bristol-Myers Squibb

Sourced by ZipRecruiter

Bristol-Myers Squibb is a world-renowned global Biopharmaceutical company headquartered in New York, NY, US. Established in 1887, the company has more than 130 years’ worth of history dedicated to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. The company operates in the healthcare industry and thrives on providing a range of pharmaceutical products and services for various medical fields, like oncology, cardiovascular diseases, and immunoscience. Notably, Bristol-Myers Squibb is known for its commitment to relentless research and innovative drug development, which has led to breakthroughs like Opdivo, one of the first immunotherapies.

Industry

Scientific research and development services and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

New York, NY, US