Medical Risk Consultant Job at Berkshire Hathaway Specialty Insurance (Atlanta, GA)

Associate Medical Risk Consultant

Berkshire Hathaway Specialty Insurance is seeking Associate Medical Risk Consult...

Location

United States , Indianapolis

Salary:

65000.00 - 85000.00 USD / Year

Berkshire Hathaway Specialty Insurance

Expiration Date

Until further notice

Requirements

1+ years of medical stop loss support experience, preferred
Knowledge of medical billing codes (ie: ICD10, CPT, HCPCS, REV, NDC)
Experience in Medical service industry (ie: medical office staff, acute care setting, home health care, insurance, stop loss)
Ability to work in high volume, rapid response environment
Ability to multi-task and shift priorities as needed
Exceptional attention to detail and strong organizational skills are imperative
Excellent verbal and written communication skills
Demonstrated excellence with Microsoft Excel
Experience with Excel
PDFs

Job Responsibility

Assist in managing the Employer Stop Loss referral mailbox
Assist with new and renewal group set up in Medical Underwriting ESL Office (Stop Loss Software) including uploading documents and entering data for identified risks
Manage Renewal Assignment report for the Medical Risk Consultant Team
weekly update of Renewal Assignment report with group sale notifications/data
Run various reports for nurses, auditors, and management as requested
Perform data review to identify pertinent data for medical risk reviews (ie: various Excel functions including pivot tables and charts
formulas
data cleaning, data sorting
report preparation for reviews)
Upload pertinent documents into AMS Profiler

What we offer

Comprehensive Health, Dental and Vision benefits
Disability Insurance (both short-term and long-term)
Life Insurance (for you and your family)
Accidental Death & Dismemberment Insurance (for you and your family)
Flexible Spending Accounts
Health Reimbursement Account
Employee Assistance Program
Retirement Savings 401(k) Plan with Company Match
Generous holiday and Paid Time Off
Tuition Reimbursement

Fulltime

Medical Device Regulatory and Quality Consultant

We are seeking a highly skilled consultant with experience in medical device and...

Location

United Kingdom , Melbourn

Salary:

Not provided

PA Consulting

Expiration Date

Until further notice

Requirements

A technical background in Engineering (systems, biomedical, mechanical, electrical, software, or related field) or Applied Science (physics, chemistry, biology, materials science, etc.)
Demonstrated prior direct experience in the design, development, or testing of medical devices and/or combination products
At least five years' experience in MedTech, pharmaceuticals, or life sciences, with a strong track record in regulated product development
Deep expertise in regulatory frameworks (FDA, EMA, MDR/IVDR, ISO 13485, IEC 62304, ISO 14971, GAMP, 21 CFR 4/ 820)
Proven ability to work cross-functionally with engineering, quality, and regulatory teams, contributing practical insights from previous technical roles
Strong problem-solving skills, troubleshooting expertise and the ability to drive technical decision-making in a highly regulated environment ensuring alignment with business and regulatory needs
Ability to manage multiple concurrent projects

Job Responsibility

Provide expertise on global regulatory requirements for medical devices and combination products ensuring compliance with FDA, EMA, MHRA, MDR/IVDR, and ISO standards
Guide processes for hardware, software, and AI-driven medical device development to ensure compliance with applicable regulatory standards and guidance, including ISO 13485, ISO 14971, IEC 62304, and related standards and guidance for AI-driven medical technologies
Advise cross-functional teams of designers, mechanical, electrical, software and usability engineers on requirements and best practices for regulatory and quality compliance
Ensure requirements traceability from user needs through design, development, verification, and validation
Lead risk management activities in accordance with ISO 14971, ensuring safety and efficacy through robust design and process controls
Develop and optimise clients’ Quality Management Systems (QMS) to streamline compliance and lifecycle management
Work closely with clients’ R&D teams, business stakeholders, and notified bodies to align project goals with industry requirements
Facilitate cross-functional collaboration, ensuring smooth integration between engineering, quality, and regulatory disciplines
Translate complex technical and regulatory requirements into actionable development strategies for medical technologies

What we offer

Health and lifestyle perks accompanying private healthcare for you and your family
25 days annual leave (plus a bonus half day on Christmas Eve) with the opportunity to buy 5 additional days
Generous company pension scheme
Opportunity to get involved with community and charity-based initiatives
Annual performance-based bonus
PA share ownership
Tax efficient benefits (cycle to work, give as you earn)

Fulltime

New

Sr. Physician Assistant -Abdominal Transplant

Under the direction of Transplant Surgery, the Sr. Physician Assistant provides ...

Location

United States , San Diego

Salary:

162530.00 - 214104.00 USD / Year ▼

UC San Diego

Expiration Date

July 14, 2026

Requirements

Must be a graduate from a physician assistant program approved by the Accreditation Review Commission on Education for the Physician Assistant (ARC-PA)
California Physician Assistant (PA) license
Current PA Certification from NCCPA
BLS/CPR certification at time of hire with commitment to get BART within six months of hire date
Minimum one (1) year of experience as a licensed Physician Assistant (PA)in transplant surgery, transplant nephrology, transplant hepatology, solid organ transplant, or adult critical care
Advanced clinical knowledge of solid organ transplant care, including post-operative management, immunosuppression protocols, transplant-related complications and rejection, and expected recipient outcomes
Demonstrated ability to independently manage complex, high-acuity transplant patients in a fast-paced inpatient setting, with evidence-based, sound clinical judgment and appropriate escalation of care
Proven expertise in rapid patient assessment, stabilization, and escalation of care in fast-paced, high-acuity clinical environments
Strong understanding of transplant-specific pathophysiology, laboratory interpretation (normal and abnormal values), and medication management for transplant populations
Serve as a liaison between patients, families and the transplant multidisciplinary team

Job Responsibility

Provides comprehensive inpatient medical management for liver and kidney transplant recipients
Independently assess, diagnose, and manage high-acuity transplant patients
Interpret transplant-specific laboratory data and diagnostic studies
Manage immunosuppression and transplant-related complications
Evaluate patients for escalation of care
Perform procedures as credentialed
Provide consultative services
Ensure accurate, timely documentation in the medical record
Present patients during daily rounds and transplant clinical meetings
Coordinate care across disciplines

Fulltime

New

Clinical Scientist Director - Late Development Oncology

Join Amgen’s Mission of Serving Patients. At Amgen, if you feel like you’re part...

Location

Portugal , Lisbon

Salary:

105822.45 - 143171.55 EUR / Year

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree and 4 years of life sciences/healthcare experience
Master’s degree and 7 years of life sciences/healthcare experience
Bachelor’s degree and 9 years of life sciences/healthcare experience

Job Responsibility

Serve as a clinical and scientific subject-matter expert for the assigned therapeutic area and disease indication, with a strong focus on protocol execution and data integrity
Contribute to medical monitoring activities and support ongoing assessment of subject-level clinical data to identify trends, risks, and emerging issues
Present information internally and externally, anticipating and actively managing problems across a broad spectrum of cross-functional teams
Provide guidance and assistance in the identification and management of collaborators, consultants, and/or Clinical Research Organizations (CROs) in completion of key projects
Work cross functionally to ensure clinical strategy is translated into the development of the study concept document, study protocol, and related documents
Ensure integrity of protocols and/or components of clinical plans and for the delivery of final protocol and its governance approval
Provide clinical input into & implementation of clinical trial(s), delivery, clinical data review, and interpretation of results
Review and analyze clinical trial data to ensure accuracy, completeness, and adherence to protocol and regulatory requirements
Conduct thorough data quality assessments in the context of a data monitoring plan to maintain high standards of data accuracy and integrity throughout the trial lifecycle

What we offer

health and welfare plans for staff and eligible dependents
financial plans with opportunities to save towards retirement or other goals
work/life balance
career development opportunities
Comprehensive employee benefits package including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
Discretionary annual bonus program
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models including remote and hybrid work arrangements where possible

Fulltime

New

IV Pharmacist - Long Term Care - Full Time

We’re building a world of health around every individual — shaping a more connec...

Location

United States , Cheshire

Salary:

55.53 - 93.08 USD / Hour

CVS Health

Expiration Date

August 04, 2026

Requirements

BS Degree in Pharmacy or Pharm.D. degree from an accredited School of Pharmacy required
Current license to practice pharmacy in good standing
3 years infusion therapy experience which MUST include clinical management of patients
At least two (2) years of long term care experience
Immunization certification or willingness to become immunization certified
Excellent organizational and time management skills
Excellent interpersonal skills
Excellent verbal and written communication skills
Ability to work independently to plan, develop and coordinate pharmacy activities
Ability to read, analyze and interpret complex topics using reasoning abilities to apply advanced mathematical concepts and draw valid conclusions

Job Responsibility

Ensure compliance with all pharmacy laws and regulations, and sterile compounding guidelines
Maintain all required IV documentation and clinical monitoring
Fully assess new patients and new orders on existing patients for appropriateness of therapy, high risk medications, allergies, adverse indications or interactions, and other potentially adverse outcomes
Thorough knowledge of prescriber/facility notification process for drug interaction, allergy, and other adverse patient safety situations
Performs accurate dose calculations based on medication, patient condition, volume and administration rates
Program infusion pumps - Consistent and ongoing clinical monitoring of all infusion patients
Thorough knowledge of medication occurrence reporting process
Have a thorough understanding of the Omnicare Long Term Care Pharmacy/Home Infusion Pharmacy Policy and Procedure Manual and internal pharmacy policies and procedures
Knowledge of other facility infusion therapy manuals if not using the Omnicare Customer Infusion Procedure manual
IV order processing only when technical support unavailable

What we offer

medical coverage
dental coverage
vision coverage
paid time off
retirement savings options
wellness programs
other resources

Fulltime

New

Social Care Worker/Residential Care Worker

As we continue to expand to provide additional services to meet the needs of tho...

Location

Ireland , Athlone

Salary:

40957.00 - 47072.00 EUR / Year

Orchard Care Group

Expiration Date

Until further notice

Requirements

Qualification at Level 7 or above in a relevant discipline and be registered as a Social Care Worker with CORU or be in the process of registering as a Social Care Worker with CORU
Full manual driving license with eligibility to drive in Ireland
Full eligibility and availability to work with us without restriction
Qualification at Level 7 or above in a relevant health related discipline, such as: Level 7 or above in Social Care and be in the process of registering
Level 7 Psychology
Level 7 in Child & Adolescent Psychotherapy
Level 7 in Counselling/Psychotherapy
Level 7 in Youth and Community or similar
Level 7 in Social Science/Social Studies
Level 7 in Family Support

Job Responsibility

Be accountable for supporting the day to day running of the service and responsible for the execution and delivery of person-centred approach
Under the general supervision of the line manager, ensure that the people we supports’ personal plan is completed in line with regulations and standards provided
Be committed to pro-actively supporting the people we support in their daily lives and choices
Ensure that all files are in line and ready for a HIQA Inspection at any given time
Engage with families, clinicians and building links in the community
Experience implementing positive support programmes
Focusing on promoting independence and community integration
Keeping up to date on Knowledge relating to current social care policies and sectoral and national changes related to disability services
To motivate, support and encourage the people we support to engage in planned activities of their choice
To take ownership and lead key working in consultation with the people we support, motivating them to engage in meaningful activities

What we offer

Competitive salary with increments
Premium rates paid on Sunday and Bank Holidays
Income Protection
4 working weeks annual leave
Comprehensive induction process
Ongoing extensive training programme
On-going mentoring and support
Continuous Professional Development support
Higher Education Bursary
Career progression opportunities

New

Physical Therapist Per Diem

Organize and deliver medically-prescribed physical therapy to restore function a...

Location

United States , Rio Rancho

Salary:

51.59 USD / Hour

UNM Hospitals

Expiration Date

Until further notice

Requirements

Bachelor's Degree
Related Discipline
NM Physical Therapist License or Temporary License
CPR for Healthcare/BLS Prov or Prof Rescuers w/in 30 days
Bilingual English, Spanish, Keres, Tewa, Tiwa, Towa, Zuni, or Navajo 1 year directly related experience

Job Responsibility

Evaluate patient to determine treatment goals
outline delivery of therapy according to assessed needs
plan therapy program involving physical means to include exercise, massage, heat, sound, water, light, and electricity
Apply methodology for evaluation of functional ability
Consult with medical staff on patient care
Educate patient in use of specialized equipment, posture control, and therapeutic procedures
Instruct caregivers on prescribed physical therapy regimen
instruct patients and caregivers on home and personal safety in various environments
Adapt therapy techniques to meet patient needs
Conduct training for medical, nursing and ancillary personnel in therapy techniques and objectives

What we offer

Sign-On Bonus
Relocation Assistance
17% Weekday Nights, 26% Weekend Nights and 15% Weekend Day shift differentials

Parttime

New

Sr Asst Mgr, Sales - AS

As a member of Baxter’s sales team, you’ll be aligned to one of our global busin...

Location

India , Gurgaon

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

B Pharma/ BSc/ Btech with Masters in Management would be add on
5 plus years of experience desired in a reputed pharmaceutical/ Medical device/ Healthcare companies in Sales
Strategic Perspective
Effectively organizes data to identify trends, problems, and their causes
Systematically evaluates opportunities and targets those with the greatest potential for producing positive results with the minimum amount of risk
Effectively articulates new and different ways of thinking and doing business
Translates concepts and ideas into actionable plans
Ability to resolve emerging issues using existing teams and/or an established network of expert consultants
Demonstrate capability for scientific, creative and strategic thinking, championing ideas for positions, and an ability to present and maintain fair-balance during scientific discussions
Stays confident when challenged, stating the rationale for one’s viewpoint clearly while listening to and respecting others right to different opinions

Job Responsibility

Creating the market for H&S and Adhesion Prevention Portfolio
Develop user base by creating awareness & Adoption for the H&S and AP Portfolio through activations in his/her territory/accounts which would include a larger regions/states example entire Delhi NCR or extended North region
Driving secondary sales through product promotion in defined territory by meeting HCPs and para medical staff
Coordinating with commercial / purchase authorities and channel partners for ensuring supply and liquidation of products
Drive awareness and adoption on Hemostat and Adhesion Portfolio amongst Healthcare professionals
Monthly account wise planning of secondary sales leading to primary sales for their territory/accounts
Weekly planning for coverage, calls and activities like NEP/RTM/OT
Monthly/quarterly sales forecast for defined territory
Quarterly activation planning
Drives adherence to SFE processes

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Select Country

Medical Risk Consultant

Job Description

Job Responsibility

Requirements

Nice to have

What we offer

Looking for more opportunities?