Senior Medical Information Specialist

SGS_JOB_3626

Business Support
 New Jersey
AMCP dossiers
FAQ documents
PharmD

Contract - 12+ months contract

Location: Nutley NJ 07110 (Hybrid in the office on Tues, Wed and Thurs) Job Description: The Senior Medical Information Specialist is responsible for meeting the medical information needs of external customers and internal business partners. He/she will respond to medical inquiries, contribute to the development of high-quality Medical Information deliverables, and will be responsible for scientific accuracy review of assigned promotional and scientific exchange materials.

Job Responsibilities:

  • Respond to medical information inquiries from health care professionals, patient/consumers, field staff, internal business partners, and other customers utilizing standard medical response documents or by creating ad hoc responses as appropriate
  • Ensure medical accuracy of advertising, promotional and scientific materials as part of Copy Review Committee and Medical Review Committee, in collaboration with Medical Information Managers and Medical Directors; and ensure the scientific information is consistent with product labeling where appropriate Monitor scientific literature for potential adverse event reports, report findings to Product Safety within established timeframes
  • Research and conduct detailed analyses of the scientific literature for Eisai marketed products, investigational compounds, competitor products/compounds, and related disease states. Contribute to communication, reporting, and storage of findings
  • Develop, review, and/or update standard medical responses, AMCP dossiers, FAQ documents, and other medical information resources
  • Provide scientific support for assigned stakeholders on ad hoc projects and/or initiatives
  • Respond to medical information inquiries from health care professionals, patient/consumers, field staff, internal business partners, and other customers utilizing standard medical response documents or by creating ad hoc responses as appropriate
  • Ensure medical accuracy of advertising, promotional and scientific materials as part of Copy Review Committee and Medical Review Committee, in collaboration with Medical Information Managers and Medical Directors; and ensure the scientific information is consistent with product labeling where appropriate Monitor scientific literature for potential adverse event reports, report findings to Product Safety within established timeframes
  • Research and conduct detailed analyses of the scientific literature for Eisai marketed products, investigational compounds, competitor products/compounds, and related disease states. Contribute to communication, reporting, and storage of findings
  • Develop, review, and/or update standard medical responses, AMCP dossiers, FAQ documents, and other medical information resources
  • Provide scientific support for assigned stakeholders on ad hoc projects and/or initiatives

Skills:

  • Advanced bioscience degree required (PharmD preferred)
  • Demonstrated scientific knowledge and expertise, Oncology experience preferred
  • Prior knowledge and understanding of US regulatory standards related to pharmaceutical manufacturers’ communications and dissemination of medical information
  • Excellent verbal and written skills, with demonstrated experience in medical writing and development of scientific communication materials
  • Superior literature database search skills, as well as expert literature evaluation and summarization skills
  • Minimum of 1-3 years of experience in pharmaceutical industry-based medical information or related discipline
  • Advanced bioscience degree required (PharmD preferred)
  • Demonstrated scientific knowledge and expertise, Oncology experience preferred
  • Prior knowledge and understanding of US regulatory standards related to pharmaceutical manufacturers’ communications and dissemination of medical information
  • Excellent verbal and written skills, with demonstrated experience in medical writing and development of scientific communication materials
  • Superior literature database search skills, as well as expert literature evaluation and summarization skills
  • Minimum of 1-3 years of experience in pharmaceutical industry-based medical information or related discipline

Education/Experience:

  • Advanced bioscience degree required (PharmD preferred)
  • Advanced bioscience degree required (PharmD preferred)

Related Jobs

Business Process Manager

Business Support
 Arizona
$65/hr on W2.
02 Years Contract + (Highest Possibilities of extension)

Location : Tucson, AZ 85755 (Onsite). The Business Process Manager (BPM) will play a critical role in driving lean methodologies and practices across the PHCS business processes. This position works with various members of the leadership team to institutionalize continuous improvement (CI) practices within the entire organization. This position will represent PHCS to serve as a champion/role model for change. This position will identify projects, lessons learned, or best practices that can be replicated for deployment in all areas. This position will focus on training stakeholders, implementing lean principles, enhancing operational efficiency, and realizing cost reductions. This role demands a proactive influencer who can inspire a culture of continuous improvement and operational excellence.

Business Process Management (BPM)
Lean Methodologies
Six Sigma
Lean Six Sigma
Continuous Improvement (CI)
Process Mapping
Change Management
Business Transformation
Process Improvement
Operational Excellence
Root Cause Analysis
Data-Driven Decision Making
Visual Management
Training & Development

Payments & Reporting Specialist

Business Support
 New Jersey
12-Month Contract — Possible Extension

location : Morristown, NJ We are seeking a detail-oriented Payments & Reporting Specialist to support fee and rebate processing, contract review, financial reporting, and operational improvements. The ideal candidate will have 2–4 years of experience in payments, contracting, data analysis, or financial operations, along with advanced Excel and reporting skills.

SAP
Tableau
Power BI
& RMUS

Project Manager II - Pharma Services

Business Support
 Arizona
$43/hr on W2.
01 Year Contract + (Highest Possibilities of Extension)

Location : Tucson, AZ 85755 (Onsite) As a Project Manager II - Pharma Services, you will be responsible for managing projects ranging from simple to complex, driving product delivery from concept through completion. The role involves developing work plans, schedules, project estimates, resource plans, and status reports while proactively managing risks, stakeholders, compliance, and continuous improvement initiatives.

Project Management
Clinical Diagnostics
Pharma Services
Biotech
Medical Devices
Product Development
Process Improvement
Cross-Functional Project Management
Resource Planning
Risk Management
CAPEX Budget Management
Data Integrity
MS Office
MS Project
Google Suite
Agile/Scrum
Stakeholder Management
Critical Path Analysis

Research Associate III - Assay Development

Business Support
 Arizona
02 Years Contract + (Highest Possibilities of Extension)

Location : Tucson, AZ 85755 (Onsite) This is an onsite position for a Research Associate II in Assay Development, requiring 4–6 years of post-college experience. The role involves conducting research, development, and manufacturing laboratory experimentation to support Ventana projects. The candidate will design, execute, and interpret experiments, prepare technical documentation and analyses, and maintain laboratory records in compliance with company policies, including GMP, GLP, and Design Control.

Assay Development
Wet Laboratory Techniques
Experimental Design & Execution
Data Analysis
Technical Documentation
GMP
GLP
Design Control
Troubleshooting
Scientific Literature Review
Process Improvement
SAFe/Agile Planning

SAP ABAP Developer

Business Support
 California
$100.00
6-7+ months Contract

Location (mandatory): Los Angeles, CA 90013 Deliver enhancements, maintenance, and ongoing support of the SAP ISU environment. Build, configure, tune and implement automation for cloud lifecycle and operational improvement. Support of the web interface used by customers to access their cloud environment. Responsible for evaluation, development, implementation, optimization, performance and configuration of customer cloud environments. Expected to establish and maintain proficiency on emerging technologies through self-study and on-the-job training. Escalate issues and defects as necessary. Work directly with escalation teams (development, network, or engineering) until incidents are fully resolved. Provide routine communication with customers on progress, status, and root cause. Work directly with architects to help reproduce and resolve issues. Knowledge of industry standards and standards organizations (e.g. ITIL, TOGAF, PMP).

SAP ABAP Development
SAP IS-U
RICEFW Development
SAP BTP / UI5
SAP IS-U Billing & Print Workbench

SAP Security Consultant

Business Support
 California
$100.00
6-7+ months Contract

Location : Los Angeles, CA 90013 Performs audit testing according to company policy and procedures. Submits audit findings as assigned. Mitigates and addresses audit findings. Implements user access controls, configuring SAP systems to mitigate security risk to organization. Creates processes and templates for implementations of SAP features. Creates documentation and templates for development within domain. Supports alignment of development practices across all SAP systems and application teams

SAP Security
SAP GRC (Governance
Risk & Compliance)
Identity & Access Management (IAM)
Audit & Compliance

QC Associate

Business Support
 New Hampshire
$44.82/hr on W2 without PTO
10 Months

Portsmouth, NH 03801 Support the Quality Control team with laboratory testing and analytical activities for work-in-process (WIP) materials, finished goods, ad hoc testing, and customer requests. This is an entry-to-junior-level opportunity suited for recent graduates with academic laboratory experience. The role requires following established procedures and instructions, maintaining accurate documentation, and supporting the QC team with daily laboratory operations and other assigned quality activities.

Quality Control
Laboratory Testing
WIP Testing
Finished Goods
Analytical Testing
cGMP

QC Associate

Business Support
 New Hampshire
$44.82/hr on W2 without PTO
10 Months

Portsmouth, NH 03801 Support the Quality Control team with laboratory testing and analytical activities for work-in-process (WIP) materials, finished goods, ad hoc testing, and customer requests. This is an entry-to-junior-level opportunity suited for recent graduates with academic laboratory experience. The role requires following established procedures and instructions, maintaining accurate documentation, and supporting the QC team with daily laboratory operations and other assigned quality activities.

Quality Control
Laboratory Testing
WIP Testing
Finished Goods
Analytical Testing
cGMP

Project Scheduler Nuclear Projects I, II, III

Business Support
 Washington
Level I - $80/hr | Level II - $95/hr | Level III - $115/hr on W2 without PTO
12 Months

Richland, WA 99354 Support Nuclear and Engineering Projects by developing, maintaining, and coordinating detailed project schedules for online work, refueling outages, forced outages, and long-range lifecycle projects. Manage schedule integration between Passport and Primavera, assist project managers with schedule development and conflict resolution, and provide accurate scheduling information for daily, outage, and future work. The role supports project planning, resource loading, risk management, budget tracking, critical path analysis, work prioritization, and schedule recovery while ensuring projects are executed safely, on schedule, within budget, and to required quality standards.

Project Scheduling
Primavera
Passport
Nuclear Projects
Outage Planning
Risk Management
Resource Loading
Microsoft Office
logo

At SGS Consulting, we go beyond resume-job matches, creating meaningful connections and pathways for individuals to thrive in defining careers.


© 2026 All rights reserved.
logologologologo