scientific specialist

The University of Iowa

<div><p>The Department of Biostatistics Clinical Trial Statistical Data Management Center is seeking Clinical Trials &amp; Data Management Research Assistant, Associate and Specialist positions, remote and hybrid work available. Responsibilities include assisting in the development of data management plans and identifying appropriate resources for research projects; assisting with designing forms to collect and track study data, subjects, drugs, biological specimens and/or procedures; assisting in the design of database management system applications and developing specifications for data collection and modules; assisting with data processing tasks including data cleaning, reconciliation, and reporting. This position will work closely with external research partners and other CTSDMC team members to determine requirements and create comprehensive solutions for data collection, verification and validation. As a member of the CTSDMC Data Management team, this position will work closely with the IT and Protocol Coordination teams to develop the databases and data entry systems. This position is responsible for mission-critical research applications and sensitive data, so attention to detail and quality are critical.</p><div><b>
Benefits Highlights:</b></div><div></div><div><br>
This is a regular, salaried position. Fringe benefit package including paid vacation; sick leave; health, dental, life and disability insurance options; and generous employer contributions into retirement plans. Complete information regarding the full benefits package may be viewed at: Benefits | University Human Resources - The University of Iowa (uiowa.edu)</div><p><b>
Application Details:</b></p><p>
To be considered for an interview, applicants must upload <b>a resume and cover letter and mark them as a &ldquo;Relevant File&rdquo; to the submission. </b>Job openings are posted for a minimum of <b>14 </b>calendar days and may be removed from posting and filled any time after the original posting period has ended.</p><p>
Successful candidates will be required to self-disclose any conviction history and will be subject to a criminal background check and credential/education verification. Up to five professional references will be requested at a later step in the recruitment process.</p><p>
This position is eligible for <b>remote or </b><b>hybrid</b> work within Iowa and will require a work arrangement form to be completed upon the start of your employment. Per policy, work arrangements will be reviewed annually, and must comply with the remote work program and related policies and employee travel policy when working at a remote location.</p><p>
Additional Information:</p><p>
Classification Title: Clinical Trials &amp; Data Management Research Assistant, Associate and Specialist</p><p>
Appointment Type: Professional and Scientific</p><p>
Schedule: 100% positions available</p><p>
Work Modality Options: on-campus/Hybrid/remote within Iowa negotiable</p><p>
Pay Level: Research Assistant 3A Research Associate 4A Research Specialist 5A</p><p>
Contact Information:</p><p>
Organization: College of Public Health</p><p>
Contact Name: Kay Shie</p><p>
Contact Email: kay-shie@uiowa.edu</p><br>
<p></p>
<div><p><b>Research Assistant:</b></p><p><b>
Required:</b></p><p>
Requires the academic knowledge of a discipline plus the ability to translate, adapt and apply this knowledge that is generally associated with a Bachelor's degree or an equivalent combination of education and experience</p><p>
Excellent written and verbal communication skills and attention to detail</p><p>
Strong interpersonal and organization skills</p><p>
Ability to apply critical thinking, technical problem solving, and analyzing system specifications</p><p>
Occasional out-of-state travel</p><p>
Knowledge and considerable experience with Microsoft Office Suite or similar software</p><p><b>
Highly Desirable:</b></p><p>
Knowledge and some experience (1 year) with database programming (e.g. SQL), or relational database systems or statistical packages (SAS or R).</p><p><b>
Desirable:</b></p><p>
Knowledge of and/or experience with Azure DevOps for development tracking</p><p>
Knowledge of 21 CFR Part 11 compliance</p><p>
Knowledge of GCP and ICH guidelines</p><p><b>
Research Associate:</b></p><p><b>
Required:</b></p><p>
Requires the academic knowledge of a scientific field including advanced study or demonstrated capacity for scientific research that is generally associated with a Bachelor&rsquo;s degree, supplemented by one or more years of progressively responsible experience in the data management field including data collection tool development and/or data cleaning or an equivalent combination of education and experience</p><p>
Excellent written and verbal communication skills and attention to detail</p><p>
Strong interpersonal and organizational skills</p><p>
Ability to apply critical thinking, technical problem solving, and analyzing system specifications</p><p>
Occasional out-of-state travel</p><p>
Knowledge and considerable experience with Microsoft Office Suite or similar software</p><p><b>
Highly Desirable:</b></p><p>
Knowledge and some experience (2-3 years) with database programming (e.g. SQL), or relational database systems or statistical packages (SAS or R).</p><p><b>
Desirable:</b></p><p>
Knowledge and/or experience with Azure DevOps for development tracking.</p><p>
Familiarity with research processes</p><p>
Experience in design and development of database system and developing specifications for applications</p><p>
Experience with group presentations</p><p>
Knowledge of 21 CFR Part 11 compliance</p><p>
Knowledge of GCP and ICH guidelines</p><p><b>
Research Specialist:</b></p><p><b>
Required:</b></p><p>
Requires the academic knowledge of a scientific field, including advanced study or demonstrated capacity for scientific research, that is generally associated with a Master&rsquo;s degree, supplemented by three or more years of progressively responsible experience in the data management field including data collection tool development and/or data cleaning, or an equivalent combination of education and experience</p><p>
Excellent written and verbal communication skills and attention to detail</p><p>
Strong interpersonal and organizational skills</p><p>
Ability to apply critical thinking, technical problem solving, and analyzing system specifications</p><p>
Occasional out-of-state travel</p><p>
Knowledge and considerable experience with Microsoft Office Suite or similar software</p><p><b>
Highly Desirable:</b></p><p>
Knowledge and experience (4-5 years) with database programming (e.g. SQL), or relational database systems or statistical packages (SAS or R).</p><p>
Experience with Microsoft PowerBI for data visualization</p><p><b>
Desirable:</b></p><p>
Knowledge of and/or experience with Azure DevOps for development tracking</p><p>
Experience conducting clinical or social science research</p><p>
Experience in design and development of database system and developing specifications for applications</p><p>
Experience with group presentations</p><p>
Knowledge of 21 CFR Part 11 compliance</p><p>
Knowledge of GCP and ICH guidelines</p></div></div>

Clinical Trials Research Assistant, Associate and Specialist positions

Johnson & Johnson

<div><p>At Johnson &amp; Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com.</p><p>
As guided by Our Credo, Johnson &amp; Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson &amp; Johnson, we respect the diversity and dignity of our employees and recognize their merit.</p><p><b>
Job Function:
</b></p>Pharmaceutical Sales<p><b>
Job Sub Function:
</b></p>Sales &ndash; Immunology (Commission)<p><b>
Job Category:</b></p>
Professional<p><b>
All Job Posting Locations:</b></p>
Cairo, Egypt<p><b>
Job Description:</b></p><p><b>
Role Title:</b> Junior Product Specialist</p><p><b>
Location:</b> Cairo/Tanta/Alexandria, Egypt</p><p><b>
Role Type: </b>Full-time</p><p><b>
Area: </b>We are recruiting Junior Product Specialists across multiple therapeutic areas, including Immunology, Oncology &amp; Hematology.</p><h3 class="jobSectionHeader"><b>
Role Purpose</b></h3><p>
The Junior Product Specialist represents Innovative Medicine in front of healthcare professionals to ensure appropriate, compliant, and evidence based use of Innovative Medicine products. The Junior Product Specialist drives patient access, product value communication, and territory performance by promoting registered products within approved indications and collaborating effectively with cross functional teams.</p><h3 class="jobSectionHeader"><b>
Duties &amp; Responsibilities</b></h3><p><b><br>
Business Growth &amp; Patient Access</b></p><ul><li><p>
Maximize patient share through strong understanding of the patient pathway and by ensuring all sales processes align with J&amp;J compliance, quality standards, and local regulations.</p></li><li><p>
Achieve territory sales and market share targets.</p></li><li><p>
Identify short and long term business opportunities in collaboration with the Market Access team and BU strategy.</p></li></ul><p><b>
Multichannel HCP Engagement</b></p><ul><li><p>
Use a multichannel approach (F2F visits, email, phone calls, presentations, etc.) to engage HCPs with the required quality and quantity in alignment with BU strategy.</p></li><li><p>
Provide accurate, timely call feedback and documentation of engagements.</p></li></ul><p><b>
Account Management &amp; Access Expansion</b></p><ul><li><p>
Conduct comprehensive account mapping, including listing processes, logistics, contracting, stakeholder mapping, and decision making pathways.</p></li><li><p>
Build long term relationships with key account stakeholders: pharmacy directors, procurement teams, tender managers, and hospital administration.</p></li><li><p>
Follow up on consumption, stock levels, tenders, and ordering mechanisms to ensure product availability.</p></li></ul><p><b>
Scientific Excellence</b></p><ul><li><p>
Maintain updated knowledge of disease areas, competitive landscape, and Janssen IBD/Immunology products.</p></li><li><p>
Promote Janssen&rsquo;s image as a scientific and digital innovator through scientific meetings and digital promotional activities.</p></li><li><p>
Achieve expected performance in scientific quizzes and training assignments.</p></li></ul><p><b>
Compliance &amp; Operational Excellence</b></p><ul><li><p>
Adhere to all J&amp;J policies, SOPs, local regulations, HCBI, FCPA, and pharmacovigilance requirements.</p></li><li><p>
Ensure accurate CRM use, sample accountability, database updates, and continuous improvement of qualitative KPIs.</p></li><li><p>
Follow global fleet safety standards and local traffic laws.</p></li></ul><h3 class="jobSectionHeader"><b>
Main Performance Measures</b></h3><ul><li><p>
Achievement of territory sales and market share targets.</p></li><li><p>
Fulfillment of BU‑aligned KPIs and Customer Interaction Excellence requirements.</p></li><li><p>
Demonstrated discipline, integrity, leadership behaviors, and Credo‑based conduct.</p></li></ul><div></div><h3 class="jobSectionHeader"><b>
Technical / Functional Skills Required</b></h3><ul><li><p>
Strong adherence to Credo values and J&amp;J leadership imperatives.</p></li><li><p>
High awareness of all business factors affecting the territory and proactive reporting of any risks.</p></li><li><p>
Strong analytical thinking, urgency, discipline, and ability to act on business opportunities.</p></li><li><p>
Collaborative team mindset and competitive drive within compliance boundaries.</p></li><li><p>
Commitment to safeguarding company image and reporting misconduct when required.</p></li></ul><h3 class="jobSectionHeader"><b>
Qualifications/Requirements</b></h3><ul><li><p>
A minimum of a Bachelor&rsquo;s degree in <b>Life Sciences, Healthcare, Medical Sciences, Pharmacy,</b> or a closely related discipline is required.</p></li><li><p>
Experience: Entry level &ndash; no previous experience required. Fresh graduates with strong potential and learning agility will be considered.</p></li><li><p>
Digital knowledge is an advantage.</p></li><li><p>
Professional proficiency in written and spoken <b>English</b>.</p></li><li><p>
Energetic approach and enthusiasm for learning new skills.</p></li><li><p>
Strong communication and interpersonal abilities.</p></li><li><p>
Adaptability and willingness to embrace change.</p></li><li><p>
Self-motivation and commitment to continuous improvement.</p></li><li><p>
Ability to work effectively within a team and contribute positively to group efforts.</p></li><li><p>
Competitiveness and a strong drive to achieve goals.</p></li></ul><p><b>
Required Skills:
</b></p><p><b>Preferred Skills:</b></p></div>

Junior Product Specialist

Prolific

<div>
 AI Trainer - Neuroscience Specialist (Remote Advisory)
 <br/>
 <br/>
 <strong>
  About Prolific
  <br/>
  <br/>
 </strong>
 Prolific is not just another player in the AI space &ndash; we are building the biggest pool of quality human data in the world.
 <br/>
 <br/>
 Over 35,000 AI developers, researchers, and organizations use Prolific to gather data from paid study participants with a wide variety of experiences, knowledge, and skills.
 <br/>
 <br/>
 <em>
  The role
  <br/>
  <br/>
 </em>
 We are seeking
 <strong>
  Neuroscience Experts
 </strong>
 to act as evaluators for a high-level AI verification project. AI models are now generating complex technical summaries, and we need specialists to ensure these outputs maintain scientific integrity and factual accuracy.
 <br/>
 <br/>
 We need experts who can navigate dense scientific literature to judge the accuracy and structural integrity of AI-generated graphical abstracts. This is a flexible, ad hoc project paying
 <strong>
  $40+/h
 </strong>
 where your technical expertise directly influences how AI understands and summarizes complex research.
 <br/>
 <br/>
 <em>
  What you'll bring
  <br/>
  <br/>
 </em>
 <ul>
  <li>
   Specialized knowledge: Deep expertise in Neuroscience
  </li>
  <li>
   Advanced Academic Credentials: you must hold a Master's or PhD in Neuroscience or a related field.
  </li>
  <li>
   Analytical Skills: history with fact-checking tasks and strong attention to detail
  </li>
  <li>
   Nice to have: Previous experience with AI-related training or evaluation tasks and a background in scientific publishing or peer review.
   <br/>
   <br/>
  </li>
 </ul>
 <em>
  What you'll be doing in the role
  <br/>
  <br/>
 </em>
 <ul>
  <li>
   <strong>
    Scientific Review:
   </strong>
   review scientific papers alongside LLM-generated graphical abstracts.
  </li>
  <li>
   <strong>
    Fact-Checking:
   </strong>
   identify issues and inaccuracies where the graphical abstract does not faithfully represent the source scientific paper.
  </li>
  <li>
   <strong>
    Expert Verification:
   </strong>
   use your domain knowledge to ensure that technical concepts are visually and textually summarized correctly.
   <br/>
   <br/>
  </li>
 </ul>
 <em>
  Please note that to qualify for this study you will be required to pass a paid skills assessment with a sample paper and graphical abstract
  <br/>
  <br/>
 </em>
 <em>
  Why Prolific is a great platform to join as a Participant
  <br/>
  <br/>
 </em>
 Joining our platform as a Prolific participant will give you the chance to influence the AI models of the future using professional legal expertise. Once you pass our assessment, you can join Prolific in just 15 minutes, and start enjoying competitive pay rates, flexible hours, and the ability to work from home.
 <br/>
 <br/>
 We've built a unique platform that connects researchers and companies with a global pool of participants, enabling the collection of high-quality, ethically sourced human behavioural data and feedback. This data is the cornerstone of developing more accurate, nuanced, and aligned AI systems.
 <br/>
 <br/>
 We believe that the next leap in AI capabilities won't come solely from scaling existing models, but from integrating diverse human perspectives and behaviours into AI development. By providing this crucial human data infrastructure, Prolific is positioning itself at the forefront of the next wave of AI innovation &ndash; one that reflects the breadth and the best of humanity.
 <br/>
 <br/>
 <em>
  Links to more information on Prolific
  <br/>
  <br/>
 </em>
 Website
 <br/>
 <br/>
 Youtube
 <br/>
 <br/>
 <em>
  Privacy Statement
  <br/>
  <br/>
 </em>
 By submitting your application, you agree that Prolific may collect your personal data for recruiting and global organisation planning. Prolific's Candidate Privacy Notice explains what personal information Prolific may process, where Prolific may process your personal information, its purposes for processing your personal information, and the rights you can exercise over Prolific use of your personal personal information.
</div>


AI Trainer - Neuroscience (Fully Remote- USA)

Prolific Academic Ltd

<div><div><div><div><div><h2 class="jobSectionHeader"><b>AI Trainer - Neuroscience Specialist (Remote Advisory)</b></h2>
<h4 class="jobSectionHeader"><b><i>About Prolific</i></b></h4>
<p>
Prolific is not just another player in the AI space &ndash; we are building the biggest pool of quality human data in the world.</p>
<p>
Over 35,000 AI developers, researchers, and organizations use Prolific to gather data from paid study participants with a wide variety of experiences, knowledge, and skills.</p>
<h4 class="jobSectionHeader"><b><i>
The role</i></b></h4>
<p>
We are seeking <b>Neuroscience Experts</b> to act as evaluators for a high-level AI verification project. AI models are now generating complex technical summaries, and we need specialists to ensure these outputs maintain scientific integrity and factual accuracy.</p>
<p>
We need experts who can navigate dense scientific literature to judge the accuracy and structural integrity of AI-generated graphical abstracts. This is a flexible, ad hoc project paying <b>$40+/h</b> where your technical expertise directly influences how AI understands and summarizes complex research.</p>
<h4 class="jobSectionHeader"><b><i>
What you'll bring</i></b></h4>
<ul>
<li><p><b>Specialized knowledge</b>: Deep expertise in Neuroscience</p>
</li>
<li><p><b>Advanced Academic Credentials:</b> you must hold a Master's or PhD in Neuroscience or a related field.</p>
</li>
<li><p><b>Analytical Skills:</b> history with fact-checking tasks and strong attention to detail</p>
</li>
<li><p>Nice to have: Previous experience with AI-related training or evaluation tasks and a background in scientific publishing or peer review.</p>
</li>
</ul><h4 class="jobSectionHeader"><b><i>What you'll be doing in the role</i></b></h4>
<ul><li><b>Scientific Review:</b> review scientific papers alongside LLM-generated graphical abstracts.</li>
<li><b>Fact-Checking:</b> identify issues and inaccuracies where the graphical abstract does not faithfully represent the source scientific paper.</li>
<li><b>Expert Verification:</b> use your domain knowledge to ensure that technical concepts are visually and textually summarized correctly.</li>
</ul><i>Please note that to qualify for this study you will be required to pass a paid skills assessment with a sample paper and graphical abstract</i>
<h4 class="jobSectionHeader"><b><i>Why Prolific is a great platform to join as a Participant</i></b></h4>
<p>
Joining our platform as a Prolific participant will give you the chance to influence the AI models of the future using professional legal expertise. Once you pass our assessment, you can join Prolific in just 15 minutes, and start enjoying competitive pay rates, flexible hours, and the ability to work from home.</p>
<p>
We've built a unique platform that connects researchers and companies with a global pool of participants, enabling the collection of high-quality, ethically sourced human behavioural data and feedback. This data is the cornerstone of developing more accurate, nuanced, and aligned AI systems.</p>
<p>
We believe that the next leap in AI capabilities won't come solely from scaling existing models, but from integrating diverse human perspectives and behaviours into AI development. By providing this crucial human data infrastructure, Prolific is positioning itself at the forefront of the next wave of AI innovation &ndash; one that reflects the breadth and the best of humanity.</p>
<h4 class="jobSectionHeader"><b><i>
Links to more information on Prolific</i></b></h4>
<p>
Website</p>
<p>
Youtube</p>
<h4 class="jobSectionHeader"><b><i>
Privacy Statement</i></b></h4>
<p>
By submitting your application, you agree that Prolific may collect your personal data for recruiting and global organisation planning. Prolific's Candidate Privacy Notice explains what personal information Prolific may process, where Prolific may process your personal information, its purposes for processing your personal information, and the rights you can exercise over Prolific use of your personal personal information.</p></div></div></div></div></div><p></p>

AI Trainer - Neuroscience (Fully Remote- St Louis)

Kraft Heinz

<div>
 The Kraft Heinz Company is looking for a Scientific and Regulatory Affairs Specialist who will support scientific and regulatory activities to help ensure products comply with applicable regulations and internal standards. This role will collaborate cross-functionally to review product formulations, ingredients, labeling, and claims; prepare and maintain regulatory documentation; monitor regulatory changes; and provide guidance to internal stakeholders throughout product development and commercialization. The ideal candidate has a strong foundation in food science and regulatory requirements, excellent attention to detail, and the ability to communicate clearly with partners across R&amp;D, Quality, Legal, and Commercial teams.
 <br/>
 <br/>
 <strong>
  Key Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Responsible for providing timely compliance input to all projects and ensure it meets and aligns with food compliance related laws, legislation, and regulations across Africa &amp; Trade markets
  </li>
  <li>
   Responsible to give compliance guidance in work streams, and to follow up, verify and validate execution of such actions by stakeholders
  </li>
  <li>
   Accountable for validating that ingredients, formulas, labelling, and claims are in full compliance with laws and regulations in markets been sold
  </li>
  <li>
   Communicate anticipated issues and provide regulatory support and compliance guidance for projects handled to the relevant stakeholders and forums
  </li>
  <li>
   Support a proactive strategic approach in regulatory function to identify, monitor, analyze early signals of upcoming regulations that might have impact in A&amp;T market, categorize them as per their likelihood and potential impact for the business.
  </li>
  <li>
   Build and maintain relationships with the relevant industrial groups and authorities to maintain awareness of new food legislations.
  </li>
  <li>
   Track- monitor and report on the completion of necessary changes that need to be done due to new regulations in order to prevent any penalties from authority.
  </li>
  <li>
   Drive cross-functional cooperation to effectively respond to regulatory related questions, challenges and issues raised for local, import and export products.
  </li>
  <li>
   Proactively identify and communicate SRA risk in any project or work stream
  </li>
  <li>
   Accountable to ensure risk assessment and mitigation plans are communicated to stakeholders
  </li>
  <li>
   Lead the registration process, collecting relevant documents, and keeping track of license expiration for the relevant SSA markets
  </li>
  <li>
   Drive a culture of scientific and regulatory affairs adherence to internal and external compliance processes and practices, driving continuous improvements opportunities
  </li>
  <li>
   Provide technical and legal labelling Information and support artwork approval process
  </li>
  <li>
   Ensure consistency and synergy in label &amp; declarations on packaging across A&amp;T markets (especially shared artworks)
  </li>
  <li>
   Scientific and regulatory affairs representation in all projects driven forums
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor&rsquo;s degree in pharmacy, Biotechnology, or Food Science
  </li>
  <li>
   5 years of experience in regulatory compliance/affairs preferably within a food, beverage, or consumer sector
  </li>
  <li>
   Experience working with Microsoft programs and system tools related to recipes and artworks
  </li>
  <li>
   Experience in translation is preferred
  </li>
  <li>
   Fluent in Arabic &amp; English, French is a plus
  </li>
 </ul>
</div>


Scientific & Regulatory Affairs Specialist – Africa & Trading

<div><div>The Kraft Heinz Company is looking for a Scientific and Regulatory Affairs Specialist who will support scientific and regulatory activities to help ensure products comply with applicable regulations and internal standards. This role will collaborate cross-functionally to review product formulations, ingredients, labeling, and claims; prepare and maintain regulatory documentation; monitor regulatory changes; and provide guidance to internal stakeholders throughout product development and commercialization. The ideal candidate has a strong foundation in food science and regulatory requirements, excellent attention to detail, and the ability to communicate clearly with partners across R&amp;D, Quality, Legal, and Commercial teams.<br>
</div><div></div><br>
<div><b>Key Responsibilities:
</b></div><ul><li>Responsible for providing timely compliance input to all projects and ensure it meets and aligns with food compliance related laws, legislation, and regulations across Africa &amp; Trade markets
</li><li>Responsible to give compliance guidance in work streams, and to follow up, verify and validate execution of such actions by stakeholders
</li><li>Accountable for validating that ingredients, formulas, labelling, and claims are in full compliance with laws and regulations in markets been sold
</li><li>Communicate anticipated issues and provide regulatory support and compliance guidance for projects handled to the relevant stakeholders and forums
</li><li>Support a proactive strategic approach in regulatory function to identify, monitor, analyze early signals of upcoming regulations that might have impact in A&amp;T market, categorize them as per their likelihood and potential impact for the business.
</li><li>Build and maintain relationships with the relevant industrial groups and authorities to maintain awareness of new food legislations.
</li><li>Track- monitor and report on the completion of necessary changes that need to be done due to new regulations in order to prevent any penalties from authority.
</li><li>Drive cross-functional cooperation to effectively respond to regulatory related questions, challenges and issues raised for local, import and export products.
</li><li>Proactively identify and communicate SRA risk in any project or work stream
</li><li>Accountable to ensure risk assessment and mitigation plans are communicated to stakeholders
</li><li>Lead the registration process, collecting relevant documents, and keeping track of license expiration for the relevant SSA markets
</li><li>Drive a culture of scientific and regulatory affairs adherence to internal and external compliance processes and practices, driving continuous improvements opportunities
</li><li>Provide technical and legal labelling Information and support artwork approval process
</li><li>Ensure consistency and synergy in label &amp; declarations on packaging across A&amp;T markets (especially shared artworks)
</li>Scientific and regulatory affairs representation in all projects driven forums<br>
<li>
</li></ul><div></div><br>
<div><b>Qualifications:
</b></div><ul><li>Bachelor&rsquo;s degree in pharmacy, Biotechnology, or Food Science
</li><li>5 years of experience in regulatory compliance/affairs preferably within a food, beverage, or consumer sector
</li><li>Experience working with Microsoft programs and system tools related to recipes and artworks
</li><li>Experience in translation is preferred
</li><li>Fluent in Arabic &amp; English, French is a plus</li></ul></div>

Lynker

<div>Overview:
<div>
Lynker Corporation is a leading provider of innovative solutions in weather and climate science. With a commitment to excellence and a passion for innovation, Lynker leverages cutting-edge technologies and scientific expertise to support the creation and delivery of improved operational weather forecasts.<br>
<br>
As part of our ongoing growth and expansion, we are seeking a dynamic and experienced Coastal Management Specialist to support NOAA&rsquo;s Office for Coastal Management (OCM). The successful candidate will work closely with state partners and organizations to support the implementation of the National Coastal Zone Management Program and the National Coastal Nonpoint Pollution Program. These two programs are authorized under the Coastal Zone Management Act and the Coastal Zone Act Reauthorization Amendments Section 6217, respectively.</div><div></div><div><br>
This position can be fully remote within the Mid-Atlantic but requires physical presence in the DC region for periodic in-person meetings at the NOAA offices in Silver Spring, MD or in Washington DC. Some additional domestic travel may be required.</div>
Responsibilities:
<div><b>
Duties of the Coastal Management Specialist will include the following:</b></div><p></p><p><b><br>
Support the Implementation of the National Coastal Nonpoint Pollution Control Program</b></p><ul><li><div><ul><li><div><ul><li><p>
Work with OCM&rsquo;s Coastal Nonpoint Program lead and EPA, and state partners as needed, to prepare decision documents regarding the approvability of a state&rsquo;s coastal nonpoint program.</p></li><li><p>
Support the development of administrative records, respond to public comments for proposed decisions in the Federal Register, develop communications plans and briefing documents regarding federal actions on state coastal nonpoint programs, and collect and review records for responses to any relevant Freedom of Information Act requests.</p></li><li><p>
Work with OCM&rsquo;s Coastal Nonpoint Program lead and OCM&rsquo;s Environmental Compliance Team to complete all necessary environmental compliance. requirements needed for decisions on state coastal nonpoint programs.</p></li></ul></div></li></ul><ul><li><p><b><br>
Support the Implementation of Coastal Zone Management Act Programs:</b></p><p></p><ul><li><p><br>
Serve as a liaison to and subject matter expert on assigned Coastal Zone Management (CZM) program(s), including: monitoring and providing appropriate financial, policy/management, and technical assistance in coordination with federal leads.</p></li><li><p>
Coordinate with NOAA&rsquo;s Federal Program Officer to negotiate, process, amend, and monitor cooperative agreements and grants, and provide technical assistance to assigned CZM programs on grants management.</p></li><li><p>
Conduct necessary environmental compliance for cooperative agreement tasks, including relevant post-award actions, and coordinate with OCM environmental compliance team for guidance and approval.</p></li><li><p>
Support implementation activities, including: review and approval of annual performance measure submissions; participation in routine evaluations of assigned state CZM programs required under the CZMA; review and recommend approval of changes to assigned state CZM programs and program enhancement strategies to the federal project leads as required under the CZMA.
</p></li><li><p>Work with OCM&rsquo;s Communities Program Manager to support projects or efforts related to the implementation of the National Coastal Zone Management Program, which may include development of funding summaries, and/or work related to the National Coastal Zone Management Strategic Plan.</p></li><li><p>
Participate and contribute to both OCM Program and Regional Teams.</p></li></ul><p><br>
</p></li><li>
</li></ul></div></li></ul>Qualifications:
<div><b>
The Coastal Management Specialist selected should have the following:</b></div><div></div><ul><li><p><br>
Master&rsquo;s degree in Environmental Policy, Marine Policy, or a related field, <b>plus</b> 3 additional years of relevant professional experience.</p></li><li><p>
Documented experience in environmental planning, policy, technical, and regulatory support for the Federal Government.</p></li><li><p>
Documented knowledge of/experience with coastal management issues, with experience specific to coastal nonpoint pollution preferred.</p></li><li><p>
Strong communication skills, including both written and oral communication.</p></li><li><p>
The successful candidate will be organized, detail-oriented, manage time to achieve project objectives to meet deadlines, and work both independently and collaboratively as part of a team.</p></li><li><p>
Ability to pass a National Agency Check and fingerprinting background check and maintain it through the duration of employment.</p></li></ul><div></div><div><b><br>
About Lynker</b></div><div></div><div><br>
Lynker is a growing, employee owned business, specializing in professional, scientific and technical services. Our continually expanding team combines scientific expertise with mature, results-driven processes and tools to achieve technically sound, cost effective solutions in hydrology/water sciences, geospatial analysis, information technology, resource management, conservation, and management and business process improvement.</div><div></div><div><br>
We focus on putting the right people in the right place to be effective. And having the right people is critical for success. Our streamlined organization enables and empowers our talented professionals to tackle our customers' scientific and technical priorities &ndash; creatively and effectively.</div><div></div><div><br>
Lynker offers a team-oriented work environment, and the opportunity to work in a culture of exceptionally skilled professionals who embrace sound science and creative solutions. Lynker's benefits include the following:</div><ul><li>
Comprehensive healthcare for the employee at no monthly cost</li><li>
Healthcare benefit covers medical, prescription drug, dental, and vision</li><li>
Personal Time Off (PTO) Policy plus paid holidays</li><li>
Highly competitive compensation plan regularly calibrated against industry and location benchmarks</li><li>
401(k) retirement plan with company-matching</li><li>
Employee Stock Ownership Plan (ESOP) &ndash; we're all company owners!</li><li>
Flexible spending accounts</li><li>
Employee assistance program (EAP)</li><li>
Short- and long-term disability insurance</li><li>
Life and accident insurance</li><li>
Tuition assistance/Training/Workforce improvement reimbursement per year</li><li>
Spot bonuses for exceptional performance</li><li>
Annual Employee Recognition Awards with bonuses</li><li>
Employee Referral Program</li><li>
Free centralized, self-directed Learning Management System to learn at your own pace</li><li>
Personalized career growth plans for every employee</li></ul><div><b>
Lynker is an E-Verify employer.</b></div><div></div><div><b><br>
Lynker is an equal opportunity employer and makes all employment decisions based on merit, qualifications, and business needs. We do not discriminate on the basis of race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), national origin, age, disability, genetic information, marital status, veteran status, or any other legally protected status under federal, state, or local laws</b>.</div><div></div><div><div><div><ul><li><br>
️ <b>Fraud Alert: Recruitment Scam Warning:</b> Lynker has been made aware of fraudulent individuals posing as Lynker recruiters and offering fake job opportunities. All legitimate Lynker job postings are listed on our official careers page. Communication from Lynker recruiters will come from an official @lynker.com email address.</li></ul></div></div></div></div><div></div>

Coastal Management Specialist

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