Grovy Developer

Job Description &ndash; Executive Assistant (EA) to MDCompany: Grovy Real Estate Developers LLC (https://www.grovy.ae/)Location: Dubai, UAEAbout Grovy Real Estate Developers LLCGrovy Real Estate Developers LLC is a fast-growing real estate development and investment company based in Dubai, delivering high-quality residential and commercial developments. With a strong focus on execution excellence, financial discipline, and strategic growth, Grovy operates in a dynamic and performance-driven environment, requiring high levels of leadership support, operational efficiency, and financial coordination.What we&rsquo;re looking for:We are seeking a highly organized, proactive, and detail-oriented Executive Assistant to provide strategic and operational support to senior leadership. The role requires strong ownership, excellent communication, financial exposure, confidentiality handling, and execution discipline.The ideal candidate will have prior experience supporting senior leadership, strong organizational skills, and exposure to finance-related coordination and reporting.What you will own and do:Act as a strategic right-hand support to the MD, ensuring seamless day-to-day functioning, prioritization, and execution excellence.Manage end-to-end executive calendar, travel, meetings, and scheduling, optimizing leadership time and focus.Serve as the central coordination hub between leadership and all internal departments, including Finance, Investments, Sales, Marketing, Projects, Legal, HR, Procurement, and Operations, ensuring:Timely flow of informationCross-functional alignmentClosure of action items.Manage direct stakeholder coordination with:Board membersInvestorsBankersJV partnersConsultantsAuditorsLegal advisors.Own end-to-end executive calendar, meeting, and travel management, optimizing leadership bandwidth.Plan and manage leadership meetings, board reviews, investor calls, and strategic discussions, including:Agenda preparationPre-read coordinationPresentation collationMoM documentationAction tracking &amp; closure.Draft, review, and manage high-level professional communication including emails, letters, reports, presentations, and confidential correspondence.Track strategic priorities, key deliverables, deadlines, and commitments, ensuring zero slippage on leadership-critical tasks.Support finance-related coordination, including:Invoice trackingExpense reportingBudget monitoringPayment follow-ups with finance teams.Maintain absolute confidentiality of sensitive leadership, financial, and business information.Provide personal assistant support to leadership, including:Personal calendar coordinationTravel logisticsPriority task handlingUrgent issue management.Proactively identify process gaps and efficiency opportunities, implementing workflow improvements and automation wherever possible.Act as a trusted confidant and execution anchor for leadership.What you will bring to us:High organizational discipline and time management excellence.Strong communication, documentation, and follow-up capability.Prior exposure to finance, reporting, or accounting coordination.Absolute confidentiality, integrity, and professional maturity.Proactive problem-solving mindset with high ownership orientation.Qualifications:Education:Bachelor&rsquo;s degree in Business Administration, Finance, Commerce, Management, or related field.Experience:4&ndash;8 years of experience as Executive Assistant / Senior Secretary / Leadership Support Role.Prior experience supporting CXOs / Directors / Senior Management.Exposure to finance coordination, reporting, MIS, or accounting workflows preferred.Job Type: Full-time

Executive Assistant (EA) to MD

RELX Group

<div></div><div><div>Clinical Analytics Specialist &ndash; MD</div><div></div><div> 
Are you a licensed MD looking to help drive innovation within our global organization?</div><div> 
About the role. We are looking for an MD to serve as our Clinical Analytics Specialist to join the Data Discovery and Enrichment Team (DDE). The Clinical Analytics Specialist will provide support for clinical decision support (CDS) product development to improve the search and discovery experience for users of products such as ClinicalKey at the point-of-care. You will have a critical role in working with the Clinical Solutions and Education business units to provide clinical analytics support and drive growth, revenue generation, and innovation.</div><div></div><div> 
About the team. This team is entrusted with the validation of extracted medical information from Elsevier corpus and electronic health care records, information retrieval, creating data for gold set generation, and participating in content enrichment workflows aiding in clinical decision support.</div><div></div><div> 
Experience</div><ul><li>
Clinical degree required (MD, MBBS,GP) Preference given to those with formal training or significant experience in evidence-based medicine, clinical research, epidemiology, biostatistics, and the application of evidence to practice.</li><li>
Experience in semantic technologies, including text mining, ontology management is a plus.</li><li>
Excellent command of the English language in both spoken and written forms is required and some level of proficiency with another language is a plus.</li><li>
Experience with medical vocabularies such as SNOMED CT and ICD-10 is beneficial, as is knowledge of ontology modeling.</li><li>
Extensive computer skill competency. Proficiency in a Microsoft Windows environment; and strong MS Word/Powerpoint skills and ability to work with templates using an electronic content management system. Visualization and dashboarding skills (e.g. using Tableau) is a plus.</li><li>
Demonstrated problem-solving ability, sense of urgency, and ability to prioritize tasks, to work simultaneously on multiple projects, and to ensure completion of editorial team projects per tight timelines.</li><li>
The Clinical Analytics Specialist should be a clinician (MD, MBBS or GP) with experience in informatics and knowledge retrieval</li><li>
Able to work with a variety of stakeholders at the mid and senior management level</li></ul><div></div><div> 
Responsibilities</div><ul><li>
Appling clinical knowledge to extract and integrate data in a healthcare environment.</li><li>
Adapting domain ontologies for information extraction, data modeling and analysis.</li><li>
Working closely with data scientists, clinicians, subject matter experts (SMEs), taxonomists, and data analysts to provide insights used in automation and applications for our businesses in health markets</li><li>
Working on the modeling, validation, and maintenance of core extracted clinical relationships to deliver an evidence-based and development of Elsevier&rsquo;s healthcare knowledge graph (H-graph).</li><li>
Providing insight for ensuring high quality of automated indexing for search &amp; discovery.</li><li>
Appling own domain knowledge and work with external clinical experts to confirm and validate clinical accuracy of content. Ensure that content is clinically accurate, current, and supported by the best available evidence from the medical literature, current guidelines, and accepted performance standards.</li><li>
Building domain specific training data sets for machine learning (ML) models used in Point-of-care products</li><li>
Predictive analytics and insights from combining big datasets in healthcare</li><li>
Participating in design, prototyping, and analytics in their day to day providing insights for algorithm codification that will improve clinical workflows and content creation.</li></ul><div></div><div> 
 Elsevier is a renowned global information analytics company that primarily focuses on providing scientific, technical, and medical (STM) research content, tools, and services. It is one of the largest publishers of academic journals and scholarly literature in the world.</div><div></div><div>
Elsevier operates in various domains, including science, technology, medicine, social sciences, and more. They publish a vast number of peer-reviewed journals covering a wide range of disciplines. These journals act as platforms for researchers and academics to share their findings and contribute to the advancement of knowledge in their respective fields.</div><div>
In addition to publishing, Elsevier offers a suite of digital solutions and services to support researchers, scientists, and professionals in their work. They provide online platforms like ScienceDirect, Scopus, and Mendeley, which offer access to a vast repository of scholarly articles, research papers, and other scientific content. These platforms often serve as essential resources for software developers seeking to stay updated with the latest scientific advancements.</div><div></div><div>
Furthermore, Elsevier offers tools and services to help researchers with tasks such as data management, article submission, and citation tracking. They also provide metrics and analytics to assess the impact and reach of scientific publications. Additionally, Elsevier hosts conferences and events to facilitate knowledge sharing and collaboration within the scientific community.</div> 
U.S. National Base Pay Range: $78,800 - $131,300. Geographic differentials may apply in some locations to better reflect local market rates.
If performed in Maryland, the base pay range is $82,800 - $137,800.If performed in New York, the base pay range is $86,700 - $144,400.If performed in New York City, the base pay range is $94,700 - $157,500.If performed in Rochester, NY, the base pay range is $78,800 - $131,300.If performed in New Jersey, the base pay range is $89,012 - $142,188.
This job is eligible for an annual incentive bonus.<div> 
We know your well-being and happiness are key to a long and successful career. We are delighted to offer country specific benefits. Click <div>here</div> to access benefits specific to your location.</div><div></div><div>
We are committed to providing a fair and accessible hiring process. If you have a disability or other need that requires accommodation or adjustment, please let us know by completing our <div>Applicant Request Support Form</div> or please contact 1-855-833-5120.</div><div></div><div>
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We are an equal opportunity employer: qualified applicants are considered for and treated during employment without regard to race, color, creed, religion, sex, national origin, citizenship status, disability status, protected veteran status, age, marital status, sexual orientation, gender identity, genetic information, or any other characteristic protected by law.</div><div></div><div>
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EEO Know Your Rights</div>.</div></div><div></div>

Clinical Analytics Specialist – MD

Elsevier

The Gill Corporation -- Maryland

<div>Who We Are:
The Gill Corporation-Maryland has long been a leader in providing high-quality, lightweight structural core materials to the aerospace, marine, construction, rail, and industrial markets. We specialize in a wide variety of structural honeycomb core materials. By utilizing broad engineering expertise along with sophisticated 5-axis CNC machining and special processing, we have the ability to deliver solutions that are responsive to customer needs.
Compensation for this role: $83,000.00 - $88,000.00 (commensurate with experience)
On-site &ndash; Monday through Friday, 7:00 AM - 3:30 PM
Summary:
The Quality Lab Supervisor effectively leads, motivates, and coordinates the activities of associates engaging in raw material testing prior to manufacturing release. This includes honeycomb block testing produced by The Gill Corporation &ndash; MD (TGC-MD) as well as customer and vendor-supplied materials.
Essential Duties and Responsibilities include the following:<ul><li>
Understands customer and industry specifications to ensure accurate testing and compliance and communicates daily work instructions and performance expectations to work group.</li><li>
Maintains open communication with Director, keeping them informed of activities within the work group.</li><li>
Ensures all documentation is complete and accurate with signatures, dates and all other required information.</li><li>
Trains new/existing associates on the required skills and operations on an ongoing basis.</li><li>
Fosters a positive work atmosphere, ensuring the work group is challenged and focused to perform the highest quality and maximum product output.</li><li>
Consistently maintains a clean and organized work area.</li><li>
Assists the current lab technicians with daily tasks such as scanning, prep work, layup, labeling, and eventually learning to complete paperwork and testing.</li><li>
Oversees receiving inspection tests of raw materials used to produce finished product.</li><li>
Coordinates visual and dimensional acceptance tests in accordance with TGC-MD and/or customer specifications.</li><li>
Generates lab test data sheets with material status and non-conformance reports.</li><li>
Performs release of accepted product and identifies released material with proper acceptance identification.</li><li>
Maintains a retrieval file system for documented objective evidence of material status.</li><li>
Develops qualification matrix for qualification of honeycomb block material.</li><li>
Performs qualification testing and generates reports showing test results.</li><li>
Manages &quot;Form B&quot; equipment sign-off sheets.</li><li>
Maintains environmental control charts in the lab and designated areas on the shop floor.</li><li>
Strictly adheres to plant safety policies, PPE requirements, and environmental health standards. Reports any unsafe work conditions to Safety Manager, supervisor, or management.</li><li>
Other duties as assigned.</li></ul>
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.
Qualifications and Education Required:<div><div><ul><li>
Minimum of Associates degree in business or equivalent lab experience required.</li><li>
Four (4) years of experience in quality testing; equivalent combination of education and experience considered, plus a minimum of two (2) years supervisory experience with accountability for staff performance and operational/process outcomes.</li><li>
Proficiency in SAP, LIMS and Microsoft Office Suite (Excel, Word, Outlook, PowerPoint).</li><li>
Acceptable vision test results (as applicable).Acceptable vision test results (as applicable).</li><li>
Must have English reading, writing and verbal communication skills sufficient to read, write, and understand and communicate the company operating procedures and policies.</li></ul><div>
</div>Physical Demands
The employee frequently is required to stand, walk, sit, reach with hands and arms, and talk or hear. While performing the duties of this job, the employee is regularly required to use hands to finger, handle, or feel. The employee is occasionally required to lift and/or move up to 35 pounds. Specific vision abilities required by this job include close vision, color vision, and the ability to adjust focus.
Benefits offered:
<ul><li>Full range of medical benefits, dental, vision</li><li>
Life Insurance</li><li>
401(K) and Profit Sharing</li><li>
Paid Vacation and 10 Paid Holidays</li><li>
Tuition Reimbursement</li><li>
Employee discounts to theme parks, attractions, shows, and more!
</li></ul>ITAR Requirement: This position requires access to information that is subject to compliance with the International Traffic Arms Regulations (ITAR) and/or the Export Administration Regulations (EAR). In order to comply with the requirements of the ITAR and/or the EAR, applicants will be asked to provide specific documentation to verify U.S. person status under the ITAR and the EAR. A U.S. person according to their definition is a U.S. citizen, U.S. lawful permanent resident (green card holder), or protected individual such as a refugee, or asylee.
The Gill Corporation is an Equal Opportunity Employer. Applicants for all job openings are welcome and will be considered without regard to race, religious creed, color, age, sex, gender identity, gender expression, genetic information, sexual orientation, national origin, religion, marital status, medical condition, physical or mental disability, military service, veteran status, pregnancy, childbirth and related medical conditions, or any other classification protected by federal, state, and local laws and ordinances.
The Gill Corporation provides reasonable accommodations. The Gill Corporation provides reasonable accommodations to qualified individuals with disabilities in accordance with the Americans with Disabilities Act and applicable state and local law. If you require accommodation in the application process, please notify the Human Resources Department.</div></div></div>

Quality Lab Supervisor - MD

Holy City Med Urgent and Primary Care

Position OverviewHoly City Med Urgent &amp; Primary Care is seeking an experienced Urgent Care Provider (MD/DO or PA-C) to join our growing, high-performing team.As healthcare in our community continues to evolve, we are committed to providing a reliable, provider-led, patient-centered alternative&mdash;focused on efficiency, quality care, and an exceptional patient experience.This is an excellent opportunity for providers who thrive in a fast-paced environment, value autonomy, and are passionate about delivering high-quality, evidence-based care.What We Offer<ul><li>Competitive compensation</li><li>Flexible scheduling options</li><li>No Sundays &mdash; strong work-life balance</li><li>Supportive clinical and administrative team</li><li>Modern, streamlined workflows</li><li>Opportunity for growth within a rapidly expanding practice</li></ul>Responsibilities<ul><li>Provide comprehensive urgent care and primary care services to patients of all ages</li><li>Evaluate, diagnose, and treat acute illnesses and injuries</li><li>Perform procedures including suturing, splinting, I&amp;D, etc.</li><li>Order and interpret labs, imaging, and diagnostic tests</li><li>Maintain accurate and timely documentation in EMR</li><li>Collaborate with clinical team to ensure efficient patient flow</li><li>Deliver an exceptional patient experience with a focus on quality and compassion</li></ul>Qualifications<ul><li>MD/DO or PA-C (active South Carolina license or ability to obtain)</li><li>Urgent care or emergency medicine experience required</li><li>Strong clinical decision-making skills</li><li>Ability to manage a high patient volume efficiently</li><li>Comfortable working independently</li><li>Excellent communication and bedside manner</li></ul>Who You Are<ul><li>You thrive in a fast-paced, high-volume setting</li><li>You value efficiency without compromising quality</li><li>You take pride in delivering thoughtful, patient-centered care</li><li>You&rsquo;re adaptable, team-oriented, and solutions-driven</li></ul>Why Holy City MedWe are a locally owned, provider-led practice built on the belief that healthcare can be both high-quality and accessible&mdash;without sacrificing the patient or provider experience.Our team is intentional about creating an environment where providers feel supported, respected, and empowered to practice medicine at a high level.Pay: $65.00 - $120.00 per hourBenefits:<ul><li>Employee discount</li><li>Malpractice insurance</li></ul>Work Location: In person

PRN Pool MD/DO or PA-C

Vital Rx

Overview You review and approve peptide therapy prescriptions through an asynchronous workflow. All patients complete full intake before reaching you. This includes medical history, contraindication screening, and peptide-specific questionnaires. Your role focuses on clinical review, safety, and approval.This role fits providers who want flexible, remote income with minimal admin work.Responsibilities<ul><li>Review patient charts submitted through the platform</li><li>Evaluate medical history, medications, and contraindications</li><li>Approve or deny peptide prescriptions based on protocol and clinical judgment</li><li>Add brief clinical notes when required</li><li>Flag any cases that need escalation or synchronous follow-up</li><li>Maintain compliance with telemedicine and prescribing regulations</li></ul>Compensation<ul><li>$10 to $15 per approved async review</li><li>High volume opportunity based on availability</li><li>Fully remote, no scheduling required</li></ul>Requirements<ul><li>Active NP, PA, or MD license</li><li>Active licenses in multiple states, priority given to providers with 5 or more states</li><li>DEA registration, if applicable to prescribing scope</li><li>Experience with telemedicine or asynchronous care preferred</li><li>Familiarity with peptides, hormone therapy, or wellness protocols preferred</li><li>Strong clinical judgment and risk awareness</li><li>Ability to review charts quickly and accurately</li></ul>Technical Requirements<ul><li>Reliable high-speed internet</li><li>Laptop or desktop computer, no mobile-only workflows</li><li>Ability to learn and use EHR and async review tools</li><li>Basic comfort with digital workflows and documentation</li></ul>Compliance Expectations<ul><li>Adhere to state-specific telemedicine laws</li><li>Follow prescribing guidelines and scope of practice</li><li>Maintain accurate documentation for every approval or denial</li><li>Prioritize patient safety over approval volume</li></ul>Ideal Candidate<ul><li>Already licensed in multiple states and looking to monetize licenses</li><li>Comfortable making fast, defensible clinical decisions</li><li>Values efficiency and structured workflows</li><li>Interested in modern, tech-enabled care delivery</li></ul>Optional Nice-to-Have<ul><li>Existing multi-state licensure across high-demand states like TX, FL, CA, NY</li><li>Background in men&rsquo;s health, weight loss, or peptide therapy</li><li>Experience with high-volume telehealth platforms</li></ul>Pay: $150.00 - $200.00 per hourApplication Question(s):<ul><li>Which states are you currently licensed in?</li></ul>Work Location: Remote

Async Telemedicine Providers Needed. NP/PA/MD

Clinical Research Center of Florida

Job Opportunity: Medical Doctor (MD) &ndash; Research CoordinatorAttention Medical Doctors! Evergreen Clinical Trials is seeking a Medical Doctor (MD) without an active medical license to join our growing research team as a Medical Doctor Research Coordinator.This role is ideal for MDs who are not currently licensed to practice clinically but are interested in gaining hands-on experience in clinical research, expanding their medical knowledge, and contributing to the advancement of medical science.Location: Peachtree Corners, GA 30092Job Type: Full-time | On-sitePay: $45,000 &ndash; $65,000 per year (based on experience) Plus performance-based bonusesAbout the RoleAs a Medical Doctor Research Coordinator, you will support Phase I&ndash;V clinical trials involving investigational medications and medical devices across multiple specialties, including:<ul><li>Psychiatry</li><li>Internal Medicine</li><li>Neurology</li></ul>All responsibilities are performed under the supervision of Principal Investigators and in accordance with FDA regulations and study protocols.Key Responsibilities<ul><li>Recruit, screen, and conduct intake assessments for potential study participants</li><li>Obtain informed consent in compliance with protocol and regulatory requirements</li><li>Conduct study visits, including:</li><li>Vital signs</li><li>Phlebotomy</li><li>EKGs</li><li>Ultrasounds</li><li>Medical histories and concomitant medications</li><li>Accurately document study data, protocol notes, and source documents</li><li>Serve as a primary point of contact for study participants</li><li>Maintain study binders, regulatory documentation, and data entry systems</li><li>Manage inventory and ordering of study supplies and equipment</li></ul>Ideal Candidate<ul><li>Medical Doctor (MD or equivalent), no active U.S. medical license required</li><li>Strong interest in clinical research and drug/device development</li><li>Excellent verbal communication and interpersonal skills</li><li>Highly organized with strong attention to detail</li><li>Ability to work independently and as part of a multidisciplinary research team</li><li>Prior clinical or research experience preferred but not required &mdash; paid training provided</li></ul>What We Offer<ul><li>Paid, structured clinical research training</li><li>Competitive base salary</li><li>Performance-based bonuses</li><li>Full benefits package:</li><li>Health insurance</li><li>Dental insurance</li><li>Vision insurance</li><li>Paid time off</li></ul>Why Join Evergreen Clinical Trials?This role offers a unique opportunity for MDs to:<ul><li>Transition into or explore a career in clinical research</li><li>Gain exposure to FDA-regulated trials</li><li>Work closely with experienced investigators</li><li>Contribute meaningfully to advancing medical treatments</li></ul>Application Questions Include:<ul><li>Have you been at your most recent job for at least 2 years?</li><li>Are you able to reliably commute to our Peachtree Corners location?</li></ul>Education Requirement<ul><li>Medical Doctor (MD) or equivalent</li></ul>Relocation Requirement: Must be able to relocate to Peachtree Corners, GA 30092 before start dateWork Location: In personWhy Join Us? This role is an excellent opportunity to gain hands-on experience in clinical research and contribute to meaningful work that advances medical knowledge. Plus, with training and mentorship from experts in the field, you&rsquo;ll have ample opportunity to grow in your career.Ready to Apply? If you're passionate about healthcare and eager to contribute to cutting-edge research, we want to hear from you!Kindly follow this link and take the assessment to submit your application: https://apply.select.wonderlic.com/QUEX9E/Clinical-Research-Center-of-FloridaJob Type: Full-timePay: $50,000.00 - $65,000.00 per yearBenefits:<ul><li>Dental insurance</li><li>Health insurance</li><li>Paid time off</li><li>Vision insurance</li></ul>Application Question(s):<ul><li>Have you been at your most recent job for at least 2 years?</li><li>Are you fluent in Spanish?</li><li>To complete the application for this position, paste this link into your browser and follow the prompt.</li></ul>https://apply.select.wonderlic.com/QUEX9E/Clinical-Research-Center-of-FloridaEducation:<ul><li>Doctorate (Preferred)</li></ul>Ability to Relocate:<ul><li>Peachtree Corners, GA 30092: Relocate before starting work (Required)</li></ul>Work Location: In person

Medical School Graduate (MD/DO) – Clinical Research Coordinator

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Executive Assistant (EA) to MD

Clinical Analytics Specialist – MD

Clinical Analytics Specialist – MD

Quality Lab Supervisor - MD

PRN Pool MD/DO or PA-C

Async Telemedicine Providers Needed. NP/PA/MD

Medical School Graduate (MD/DO) – Clinical Research Coordinator