Scientific Publication Manager, Oncology

SGS_JOB_1090

Scientific
Remote
Oncology
Scientific
Medical
Publications
Scientific Communications
Medical Affairs
CONSORT
ICMJE
GPPs

Contract - 10 Months (Contract, Possible extension of 1 year)

The role “Scientific Publication Manager –Global Scientific Communications/Publications, Oncology” reports into the Global Medical Oncology team that is part of the Medical Specialty Care organization serving as a supporting partner to the Publications Lead. This role will work cross-functionally with commercial, regulatory, clinical, and market access on therapeutic solutions to support patients’ needs. Within our Global Medical Oncology team, we are committed to advance transformative therapies to help improve outcomes and impact the lives of people living with many different types of cancer. Global Scientific Communications/Publications, Oncology.

Job Responsibilities:

  • The (Senior) Scientific Publication Manager, Global Scientific Communications, Oncology is accountable for the development and execution of scientific publications activities for Hematology/Oncology. Involvement with publication’s development may include reviewing manuscript drafts and collaborating with the therapy area publications lead to align the strategy on data dissemination. Demonstrate exceptional project management expertise, including the ability to drive various initiatives at a time, implement processes, and drive results in a fast-paced, multi-stakeholder environment. Job duties are subject to evolution, potentially encompassing responsibilities beyond those explicitly outlined in the initial description.

Skills:

  • Ability to manage multiple projects simultaneously, thinks critically, and adheres to deadlines.
  • Demonstrate track record in building and maintaining a network of internal and external experts, experience in working across and building effective partnerships
  • Result orientation and ability to drive positive outcomes and impact through excellence in execution
  • Effective stakeholder management and ability to create powerful relationships and networks
  • Work effectively in a matrix environment, tactful and values teamwork and collaboration across functions
  • Excellence in solving problems while exhibiting superior judgment and a balanced, realistic understanding of issues
  • Excellent communication skills both written and oral, including strong presentation skills
  • Ability to manage competing priorities and projects, requiring an excellent ability to prioritize and manage expectations
  • A “lifelong learner” who consistently seeks opportunities to learn
  • Absolute commitment to a culture that operates with high ethical standards and strives to exceed all goals and objectives
  • Excellent interpersonal and communication skills, written and verbal; comfortable in leading presentations
  • Knowledge of industry guidelines pertaining to data dissemination (e.g., CONSORT, ICMJE, GPPs) and interactions with health care providers (e.g., PhRMA Code, AdvaMed guidelines)
  • Experience in supervising and managing medical writing tasks and tools, including electronic tools

Education/Experience:

  • Medical / Scientific / Clinical background in Oncology
  • Demonstrated successful experience in Scientific Communications/Medical Affairs within Pharma / Biotech industry
  • Experience managing publication agencies Budget and forecasting experience
  • Medical / Scientific / Clinical background in Oncology
  • Demonstrated successful experience in Scientific Communications/Medical Affairs within Pharma / Biotech industry
  • Experience managing publication agencies
  • Knowledge of industry guidelines pertaining to data dissemination (e.g., CONSORT, ICMJE, GPPs)
  • Advanced scientific or clinical degree in the life sciences (e.g.Ph.D., Pharm.D.)

Related Jobs

Logistics Specialist III

Scientific
 New Hampshire
12 Months

The Logistics Sampling Associate is responsible for taking samples of incoming raw materials.

sample testing
Cgmp
SOP

Deviation investigator

Scientific
 Texas
6 months

Location ; Houston TX. The Deviation Investigator/Initiator Level III is responsible for the initiation, investigation and completion of Minor and low/medium severity Major process deviations unassisted, and the supervised completion of high severity Major and Critical process deviations with the aim at identification of root cause, determining Product Quality Impact (PQI) and implementation of corrective actions to prevent recurrence

Deviation
investigation
capa
documentation

Microbiologist II

Scientific
 Florida
12 months

Location : 4910 Savarese Circle Tampa FL USA 33634 Contract : 12 months Looking for a person with quality control experience and Water/microbial testing.

Microbiological testing
water testing
quality control
CAPA

QC Analyst III

Scientific
 New Hampshire
12 Months (Possibilities of Contract Extension)

The Quality Control Technical Transfer Analyst 3 will act as a team member of the Quality Control department to support production by contributing to the completion of the technical transfer activities. Also participate in quality testing for customer in-process, final product testing, and stability studies when needed.

A280
CE-SDS
icIEF
ELISA
SoloVPE
qPCR
GMP Quality Systems (TrackWise
LIMS)
Quality Records (Deviations
CAPA
Change Control)
Test Methods

Marketing Automation Support

Scientific
Remote
Contract (mandatory): 07 Months + (Possibilities of Contract Extension)

We are seeking a Marketing Automation Support professional to assist our client with various activities related to Email Marketing Campaigns, Personalization Campaigns, and A/B Testing using Adobe Marketo. The ideal candidate will have extensive experience in B2B marketing automation and a strong understanding of database management.

Key Skills (mandatory): Marketo
B2B Marketing Automation
Salesforce
Data Hygiene
HTML
CSS

Equipment Validation Specialist IV

Scientific
 New Hampshire
09 months + (Possibilities of Extension)

The Equipment Validation Specialist IV plays a crucial role in ensuring that all critical GMP equipment and systems are validated and maintained in compliance with user requirements, process parameters, and global regulatory guidelines. This position provides scientifically sound documented evidence to Operations, Quality Assurance, and regulatory bodies that systems and processes will perform as required, supporting a quality, compliant manufacturing environment.

Equipment Validation
GMP Compliance
Validation Protocols
Quality Systems
Biopharmaceutical Manufacturing
Validation Maintenance
SOP Reviews
TrackWise
Project Management
Troubleshooting
Technical Support

Equipment Validation Specialist III

Scientific
 New Hampshire
09 months + (Possibilities of Extension)

The Equipment Validation Specialist is responsible for ensuring that all critical GMP equipment and systems are validated and maintained in compliance with user requirements, process parameters, and global regulatory guidelines. This role provides scientifically sound, documented evidence to Operations, Quality Assurance, and regulatory bodies, supporting a quality, compliant manufacturing environment.

Equipment Validation
GMP Compliance
Validation Protocols
Quality Systems
Biopharmaceutical Manufacturing
Validation Maintenance
SOP Reviews
TrackWise
Data Integrity
Technical Support
Troubleshooting

Analytical Validation Specialist III

Scientific
 New Hampshire
Full-Time

The Analytical Validation Specialist III role focuses on supporting validation activities for analytical systems, such as software updates, new system introductions, and system decommissioning. This individual collaborates closely with senior specialists and other teams to ensure high-quality performance and compliance with industry standards. The role involves troubleshooting, executing qualifications, and supporting system changes while ensuring data integrity and quality systems adherence.

Analytical Equipment
Validation
Data Integrity
Quality Control
Troubleshooting
cGMP
Process Validation
Microsoft Office

QC Analyst II

Scientific
 Texas
05 months + (Possibilities of Extension)

The QC Analyst II will support the Quality Control, Microbiology Safety Team by performing bioburden, microbial enumeration, endotoxin, sterility testing, and other microbiological assays. The role will assist with OOS investigations, maintaining laboratory equipment, and ensuring compliance with cGMP regulations. The ideal candidate will have experience with USP testing methods and a background in microbiology.

Attention to Detail
Time Management
Organization
Microbiological Assays
Endotoxin Testing
Sterility Testing
Bioburden
BacT/Alert
logo

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

Our Services

Contingent Workforce Solutions

Strategic SOW Services

Payroll Solutions


2025. All right reserved.
logologologologo