Senior Public Affairs Specialist Job at Barbaricum (Fort Detrick)

Public Affairs Specialist, Senior

The key to an organization’s growth is strong stakeholder communication that rep...

Location

United States , Fort Meade

Salary:

77600.00 - 176000.00 USD / Year

Booz Allen Hamilton

Expiration Date

Until further notice

Requirements

10+ years of experience as a DoD Public Affairs Specialist
Knowledge of verbal, written, social, and visual communications concepts, principles, policies, practices, methods, applications, techniques, standards, and trends
Ability to write, edit, and prepare news releases and programs for press, radio, and television, including the organization and layout of publications used in the public affairs program, ensuring conformity to command and government guidelines
Active TS/SCI clearance
willingness to take a polygraph exam
Bachelor's degree

Job Responsibility

Design, develop, produce, and advise on a variety of internal and external communication materials and media that support the planning and implementation of a comprehensive public affairs program
Develop creative solutions to complex problems
Shape and nurture relationships with team members, stakeholders, and clients to inform interested audiences
Oversee and author news releases, programs for press, and responses to information requests on assigned programs from the news media, specialized groups, or the public
Inform key audiences through words, images, and sound with a wide range of verbal, written, social, and visual communications concepts, principles, policy, practices, methods, applications, techniques, standards, and trends

What we offer

Health, life, disability, financial, and retirement benefits
Paid leave
Professional development
Tuition assistance
Work-life programs
Dependent care
Recognition awards program

Regulatory Affairs Specialist

Regulatory Affairs - office based - Bogota. ICON plc is a world-leading healthca...

Location

Colombia , Bogota

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Bachelor's degree in Pharmaceutical Chemist or next to graduate required
Minimum 1 year of experience in regulatory area within the pharmaceutical or biotechnology industry
Knowledge or awareness of current regional guidelines and regulations is preferred
Technical knowledge in the preparation of a dossier is desirable
Prior experience using computerized information systems required: PC Windows, word processing and electronic spreadsheets
Advanced English level

Job Responsibility

Manage activities associated with obtaining initial, amendment and other central authority approvals i.e. Regulatory Agency (RA), and any other central authorities for the assigned country/ countries
Perform submission and maintenance of new health records, renovations and modifications to keep the products on the market according to the strategic plan established by the company, current Colombian laws and current local health legislation in accordance with the corporate guidelines and policies, procedures and premises
Review of promotional materials for products for human use of their therapeutic line(s) in Veeva Vault or current tool
Perform submission and monitoring of products for human use of their therapeutic line(s) in procedures such as: PSUR, DSUR, RMPs, and safety information according to current Colombian regulations
Back-up to the Head of Regulatory Affairs and analysts of records in the procedures of INVIMA in order to guarantee the operation of the area
Ensure that IP labels are in adherence to country requirements and submitted where applicable
Support the senior level regulatory staff/country consultant in the maintenance of accurate, up-to date Country Knowledge repositor
Contribute to the maintenance and collection of regulatory intelligence by ensuring that tools such as the Country Knowledge Repository and the Country Fact Sheets are up-to-date and communicate new information or changes to the Regulatory Intelligence Consultant team
Preparation of electronic regulatory submission of post-registration requests, HMPs, Labeling notifications, additions, publication corrections and database corrections, among other petitions to be field at MoH
Follow-up on the status of the regulatory submissions (paper dossiers) from dispatch to the receipt of proof of protocol

What we offer

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others

Fulltime

Marketing Specialist Senior

The Senior Marketing Specialist ("the Specialist") is responsible for leading co...

Location

United States , Irving

Salary:

Not provided

CHRISTUS Health

Expiration Date

Until further notice

Requirements

Bachelor's Degree

Job Responsibility

Lead coordination of marketing and communication activities for CHRISTUS entities and departments/initiatives
Assist with regional/entity marketing plan development and customer relationship management (CRM) program development
Coordinate system health campaigns or other branding/marketing messaging for regional use
Coordinate with system ad agencies and graphic designers for campaign development and/or order form development
Understand CRM strategies for deployment at the regional/entity level
Identify customer segments and engagement activities
Utilize third party contracted applications
Assist Director of CRM with regional/entity educational opportunities/meetings and coordination of plug-in products
Serve as primary department contact for Project Management of internal system department requests
Manage outside vendors, ad agencies, graphic designers, production companies, printers and related contracted resources

Fulltime

Senior Communications Specialist

This role is at Spirit AeroSystems, Inc., a wholly owned subsidiary of The Boein...

Location

United States , Wichita

Salary:

93100.00 - 142700.00 USD / Year

Boeing

Expiration Date

Until further notice

Requirements

Bachelor’s Degree
10+ years of related experience developing and implementing communications plans and campaigns
Exceptional writing and editing skills
Ability to manage multiple, high-priority projects simultaneously
Candidates must be able to obtain and maintain a DoD Security Clearance
Successful candidates must be able to secure Program access approval

Job Responsibility

Develop robust employee engagement plans, including manager programming, to ensure all employees are aligned with Spirit Defense business goals and objectives
Develop external programming to meaningfully support business development activities, including but not limited to trade shows, speaking engagements, media relations, and other creative approaches
Provide communications support and recommendations to ensure the effectiveness of Spirit Defense compliance initiatives
Lead planning, coordination, execution, and measurement of results for communications initiatives
Manage Spirit Defense digital platforms (website, social media)
Budget and vendor management responsibilities as required
Ability to travel at a projected rate of 10% and work flexible hours as business needs dictate

What we offer

Competitive base pay and variable compensation opportunities
Opportunity to enroll in a variety of benefit programs, generally including health insurance, flexible spending accounts, health savings accounts, retirement savings plans, life and disability insurance programs, and a number of programs that provide for both paid and unpaid time away from work
Generous company match to your 401(k)
Industry-leading tuition assistance program pays your institution directly
Fertility, adoption, and surrogacy benefits
Up to $10,000 gift match when you support your favorite nonprofit organizations
Development programs
$5,000 state of Kansas Aviation tax credit for up to five years (eligibility criteria apply)

Fulltime

Senior Pharmacovigilance Specialist

The Local Pharmacovigilance Specialist is responsible for the execution of tasks...

Location

Ukraine , Kyiv

Salary:

Not provided

Cencora

Expiration Date

Until further notice

Requirements

Professional education or University degree in Life Science preferred but not essential
Basic understanding/knowledge in the field of pharmacovigilance and medical information
Ability to prioritize and manage own time and tasks
Ability to manage internal and external (client) relationships on operational / day-to-day working level as well as client's team lead level
Good communication skills (written and verbally)
capability to point out issues and provide potential options for solution in the area of expertise
English business fluent

Job Responsibility

Data entry and quality control of Individual Case Safety Reports (ICSR) of adverse drug reactions deriving from clinical trials, spontaneous reporting systems and the literature
reporting of ICSRs to the competent authorities
Support in the generation, processing, documenting, and tracking of follow-up requests
Screening and documentation of scientific literature regarding safety relevant publications
Assist in the creation of periodic reports PSURs (Periodic Safety Update Reports), DSURs (Development Safety Update Reports), PADERs (Periodic Adverse Drug Experience Reports), risk management plans and signal detection reports
Interact with customers as needed (e.g. meetings, client visits, day to day case processing, etc.)
PSMF maintenance
Contribute to/review QA documents such as Working Instructions, SOPs, Working Procedures, templates, project metafiles, etc. for pharmacovigilance projects
Prepare for and participate in internal and external audits/inspections
Training new colleagues in relevant tasks

Fulltime

Senior QA/RA Specialist

The primary role of Quality Assurance function is to ensure that management syst...

Location

United Kingdom; Ireland , Harrogate; Dublin

Salary:

Not provided

ResMed

Expiration Date

Until further notice

Requirements

Bachelor's degree (technical or software background preferred) from four year college or university
at least one year of professional experience in regulatory affairs or in quality management systems relating to medical devices
four (4) to five (5) years related experience or equivalent education and experience
Strong experience or exposure across Quality Systems (ISO 13485) / Design and Development of Medical device software (IEC 62304 environment)/ Supplier quality / Medical Device Regulation (MDR 2017/745)
Good Knowledge of ISO 13485 standard and Medical Device Regulation (MDR 2017/745)
Ability to exercise judgment
Good communication, planning and organizational skills
Proactive
able to provide initiative, ownership while working through uncertainty
Self-starter, with the ability to work with minimal supervision and with a sense of urgency

Job Responsibility

Role of Management Representative (ISO 13485)
Ensure the processes needed for the Quality Management System are effectively defined, documented, implemented and maintained
communicate and report on the performance and effectiveness of the QMS and any need for improvement to the senior management team and all other company personnel
Ensure the promotion of awareness of applicable regulatory requirements and quality management system requirements throughout the organization
Coordinate and execute to support QMS activities
Ensure complaint handling / investigations, CAPA, Nonconformities, are processed and resolved in a timely manner
Suppliers’ management (including evaluation, monitoring, quality agreements)
Design and Development activities
Change control
Internal / external / supplier audits

What we offer

All employees benefit from a bonus plan
Working from home flexibility
Access to a referral bonus
Access to ResMed's preferred shareholding programme
Internal career opportunity

Fulltime

Senior Risk Functional Specialist

Payment Risk Operations is at the heart of what makes Airbnb a place where anyon...

Location

United States

Salary:

82000.00 - 96000.00 USD / Year

Airbnb

Expiration Date

Until further notice

Requirements

Minimum of 3+ years professional experience in fraud, abuse, or cybercrime investigations
Minimum of 1+ years professional experience related to stored value risk (e.g. gift cards, coupons, credits, incentives)
Detail-oriented, highly analytical, and strong project management skills
Ability to understand opposing points of view on highly complex issues
Strong ability to gather information from various internal sources
Capacity to draw actionable insights from dashboards and reports
Risk policy creation and/or administration experience
Basic SQL
Experience with data visualization and business intelligence tools (e.g. Tableau, Superset)
CFE or equivalent certifications

Job Responsibility

Oversee operational procedures and escalations related to stored value payment products (e.g. gift cards)
Review performance metrics for business and vendor feedback
Work with operational stakeholders and cross-functional partners to enact change to improve products and processes
Apply Airbnb core values in all work
Protect community by reviewing and making exceptional decisions for platform exemptions
Own incident resolution of risky pay-in procedures from escalation to closure
Navigate complex operational issues by partnering with Legal, Public Affairs, and other teams to respond to regulatory inquiries
Tell the story through data by drafting business requirements and concept briefs

What we offer

Bonus
Equity
Benefits
Employee Travel Credits

Fulltime

Senior Patient Safety Specialist

Location

Philippines , Manila

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Expert knowledge of drug safety regulations and pharmacovigilance processes
Strong analytical and problem-solving abilities
Excellent communication and presentation skills
Superior organizational and time management capabilities
Proficiency with pharmacovigilance systems and databases
Proven experience in safety case management and regulatory reporting
Proficiency with safety databases and data analysis
Strong knowledge of ICH guidelines and regional requirements
Demonstrated mentoring abilities and process improvement skills
Experience in pharmaceutical or healthcare environments

Job Responsibility

Maintain expert-level knowledge of safety profiles, labeling, and global regulations
Lead development of project-specific procedures and workflows
Provide technical guidance to junior team members
Prepare for and participate in audits and inspections
Analyze metrics and drive continuous improvement
Collaborate with cross-functional teams on safety deliverables
Identify risks and recommend mitigation strategies
Ensure compliant documentation and archiving
Lead project management including safety procedure development and database setup
Coordinate ICSR processing workflows and perform case assessment (seriousness, causality, expectedness)

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Senior Public Affairs Specialist

Job Description

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