clinical dermatologist

La Fami Medical Complex

Iam urgently hiring dermatologist.DOH RequiredJob Types: Full-time, Permanent, FresherPay: AED1.00 - AED2.00 per month

Dermatologist

San Marcus Research Clinic Inc.

Job Summoary:Our premier clinical research facility is seeking a board-certified or board-eligible Dermatologist (MD/DO) to serve as a Principal Investigator (PI) or Sub-Investigator (Sub-I) for upcoming and ongoing dermatology clinical trials. The ideal candidate will oversee the safety of study participants, ensure strict protocol adherence, and evaluate clinical efficacy endpoints (such as skin assessments, biopsies, and lesion tracking) for novel therapeutic compounds.Key Responsibilities:<ul><li>Serve as Principal Investigator or Sub-Investigator for Phase I&ndash;IV dermatology clinical trials in accordance with ICH/GCP guidelines and FDA regulations.</li><li>Conduct specialized clinical skin assessments, efficacy ratings, adverse event evaluations, and protocol-required physical exams.</li><li>Review protocol inclusion/exclusion criteria to confirm patient eligibility and manage the informed consent process.</li><li>Perform minor in-office research procedures if dictated by the protocol (e.g., punch biopsies, photography, skin scrapings).</li><li>Review laboratory results, ECGs, and other diagnostic data to monitor participant safety.</li><li>Collaborate with Clinical Research Coordinators (CRCs), data managers, and pharmaceutical sponsor monitors (CRAs) during site visits and audits.</li></ul>Strict Educational &amp; Licensing Requirements:To satisfy federal regulatory mandates and sponsor oversight, applicants must possess and maintain all of the following credentials:<ul><li>Medical Degree: Doctor of Medicine (MD) or Doctor of Osteopathic Medicine (DO) from an accredited institution.</li><li>Active License: Current, unrestricted Medical License in the state of practice.</li><li>Board Certification: Board Certified or Board Eligible in Dermatology (American Board of Dermatology or American Osteopathic Board of Dermatology).</li><li>Prescribing Authority: Active Federal DEA registration and state controlled substance license (if applicable).</li><li>Education History: Must provide a complete Curriculum Vitae (CV) documenting all post-graduate training, including Internship, Dermatology Residency, and any specialized Fellowships.</li></ul>Preferred Qualifications:<ul><li>Prior experience in clinical research operations, pharmaceutical trials, or working with a Clinical Research Organization (CRO).</li><li>Active ICH/GCP (Good Clinical Practice) certification (training can be provided upon hire).</li><li>Experience with standard clinical trial data capture systems (EDC/IRT).</li></ul>Join us in making a difference through innovative clinical research!Job Type: Full-timeAbility to Commute:<ul><li>Miami Lakes, FL 33014 (Preferred)</li></ul>Ability to Relocate:<ul><li>Miami Lakes, FL 33014: Relocate before starting work (Preferred)</li></ul>Work Location: In person

Dermatologist (MD/DO) for a Clinical Research

Bubble Skincare

<div><h4 class="jobSectionHeader">Job Title: Social + Affiliate Commerce Specialist 
Location: New York, NY (Hybrid, 4x Week In-Office) 
Reports To: Senior Director Digital + Ecommerce 
Compensation: $90,000 &ndash; $130,000 
Type: Full-time</h4>

About Bubble 
Bubble is a fast-growing skincare brand that's dermatologist-approved, clinically tested, and designed to bring clean, effective beauty to the next generation. We're redefining what skincare means for Gen Z and beyond&mdash;with innovative formulas, transparent messaging, and a fresh, bold approach to community-driven beauty.

About the Role 
We're looking for a Social Commerce and Affiliate Marketing Specialist to own and optimize Bubble's TikTok Shop and affiliate programs across digital commerce platforms. This role will focus on managing the day to day promotions, merchandising, creators and strategy for our TikTokShop and affiliate creators including the conversion of Bubble's ambassador community into active sellers. You sit at the intersection of content, creator/affiliate management, live shopping, and commerce operations, and you are accountable for the channel's growth. You'll partner closely with our eCommerce, organic social, retail sales, and marketing teams to maximize digital performance while staying true to our brand.

What You'll Do
<ul>
<li>Commerce Operations</li>
<li><ul><li>Own Seller Center day to day: catalog, listings, promotions, and shop health metrics.</li>
<li>Monitor and protect unit economics &mdash; commission, fulfillment, returns, ad spend, and COGS &mdash; so growth is margin-aware, not vanity GMV.</li>
<li>Coordinate with operations on fulfillment and returns, and ensure all product claims meet platform and regulatory compliance standards.</li>
<li>Manage the TikTokShop specific content, promotional strategy, affiliate seeding/sampling program and shop merchandising.</li>
</ul></li><li>Content Creation</li>
<li><ul><li>Build and run a repeatable engine of shoppable short-form content &mdash; own and seeded &mdash; at a cadence of multiple videos per day.</li>
<li>Develop derm-led content formats (ingredient education, before/after with clinical claims, routine builds) that leverage Bubble's advisory board and clinical positioning.</li>
<li>Maintain a clip library that feeds the affiliate program and live shopping.</li>
<li>Partner with social marketing + creative teams to produce content specific for selling.</li>
</ul></li><li>Creator &amp; Affiliate Program</li>
<li><ul><li>Build and manage a social selling affiliate program: a curated, managed cohort of macro and micro derm, beauty and lifestyle creators.</li>
<li>Convert a segment of Bubble's 100,000-person ambassador community into active TikTok Shop affiliates.</li>
<li>Design and manage commission structures, seeding, sample logistics, and creator briefs.</li>
<li>Track attributed GMV per creator, conversion rate on creator-driven product visits, AOV by tier, and video-to-purchase latency.</li>
</ul></li><li>Live Shopping</li>
<li><ul><li>Stand up and scale a live shopping cadence, hosting and co-hosting with creators.</li>
<li>Anchor live events to product launches, bundles, limited offers, and major promotional windows.</li>
<li>Own the live ops playbook: scheduling, run-of-show, offers, and post-live repurposing.</li>
</ul></li><li>Digital Affiliates</li>
<li><ul><li>Align TikTokShop for on-going digital commerce programs and optimize reach across all digital touchpoints.</li>
<li>Partner with Amazon agency to support Amazon affiliate strategy and it is consistent with other digital channels.</li>
<li>Partner with community and influencer teams to optimize paid creators for reach and CVR.</li>
</ul></li>
</ul>What You Bring
<ul>
<li>You have built or scaled a creator/affiliate program on TikTok Shop for a beauty, wellness, or CPG brand</li>
<li>You are fluent in TikTok Shop affiliate mechanics: creator marketplace, commission tiers, sample seeding, target collaborations, and open vs. managed program design.</li>
<li>You understand commission economics and can grow GMV without eroding margin.</li> 
</ul>
Nice to Have
<ul>
<li>Experience in the beauty, skincare, or CPG industry 
Existing beauty-creator relationships, experience converting community/ambassador bases into affiliates, or prior work with derm- or clinically-positioned brands.</li>
<li>Experience with budget management and multi-retailer campaign planning</li> 
</ul>
Why You'll Love Working Here
<ul>
<li>Join a dermatologist-approved, clinically tested skincare brand redefining beauty for Gen Z</li>
<li>Be part of a high-growth team shaping Bubble's retail footprint across Amazon and top retail partners</li>
<li>Competitive salary, benefits, and product perks</li>
<li>A collaborative, mission-driven culture that values creativity, data, and innovation</li></ul></div>

Social Commerce Specialist

Swiss American CDMO

<div>Position Summary: As a key ambassador for Swiss American CDMO (SA), the Client Services Manager II (CSM II) plays a pivotal role in fostering and maintaining strong client relationships. The CSM II is accountable for ensuring client satisfaction with SA's finished goods and services, acting as the primary point of contact throughout the entire client lifecycle. This role demands a proactive and collaborative approach, requiring the CSM II to proactively communicate project status, anticipated changes, and effectively guide clients through all phases of the finished goods production process.
Essential Duties and Responsibilities:<ul><li>
Process Management / Set-up of Client Account to the SA process to maximize commercialization success:</li></ul><ul><li>
Be the subject matter expert on the SA process. Provide necessary internal information re: company&rsquo;s capability, capacity, technical information transfer, etc. for drug and medical device development.</li>
Be the internal client advocate <li>- know client strategy and communicate effectively to enable internal SA people and process to deliver. CSM II must be able to help direct the working teams and resources, anticipate and mitigate potential delays, while never losing sight of the responsibility to SA to deliver on time and on budget.</li><li>
Capable of handling 5-8 clients, and 2-4 prospects and/or leads &ndash; with limited supervision/assistance. Timeline on managing quantity and complexity of client roster is earned post initial training and demonstration.</li><li>
Serve as the hub within SA to critical internal departments e.g., RID, Quality, Regulatory, Production, Shipping, Procurement, and other groups. Drive internal discussion and alignment on change management and when necessary, involve subject matter experts in client discussions.</li><li>
Be an active contributor to Swiss American Site Objectives and contribute to department&rsquo;s role in the Quarterly Management Review, Forecasting, and other important client services deliverables.</li><li>
Maintain current project-related information in Company systems.</li><li>
Be able to effectively discern when to escalate concerns to Management.</li><li>
Other duties may be assigned.
</li><li>Customer engagement and Communications:<ul><li>
With limited supervision, the CSM II will maintain regular, frequent client interactions, based on demand; requires timely (no later than 24 hours following request or contact) and accurate response to all client correspondence.</li><li>
Professional client communication always: written, verbal, video, in person as needed.
</li><li>CSM II must know the client products. Product Management experience is critical here to know key product ingredients, claims, unique benefits, and points of differentiation from competitive brands. From a business perspective, CSM II must know the clients&rsquo; business drivers, financial implications, and channel strategies (particularly those that involve physicians (e.g., Dermatologist) or provider (e.g., Clinics).</li><li>
Ability to effectively present information and respond to questions from internal and external Management, Customers, Clients, and cross-functional colleagues. Ability to draft client ready reports, presentations, and analysis.</li><li>
Must be comfortable and confident in articulation of the Swiss American CDMO story. The history, points of differentiation and support to drive corresponding quotation/proposals or capabilities presentations.</li><li>
Other duties may be assigned.
</li><li>Utilize business insights and understanding of healthcare market, customer business drivers to optimize go to market strategy within the SA infrastructure:<ul><li>
Understand client&rsquo;s business; healthcare market drivers of that business; product requirements; and potential adjacencies to anticipate and manage product demand needs.
</li><li>Provide client-oriented solutions with alignment across the organization to deliver ON TIME completion of order.</li><li>
Understand client product strategy and roadmap for growth in detail and be prepared with scenario building options that are specific to each customer and their industry/market. Understand potential client healthcare reimbursement models, channels, and potential areas of growth and risk.
</li><li>Analyze and interpret reports for weekly and monthly reporting requirements of customer &ndash; with limited supervision.</li><li>
Other duties may be assigned.
</li></ul></li><li>Manage financial overview of each client account to drive the SA business forward and with success:<ul><li>
Proficient in Excel, specifically in the ability to calculate figures indicating and assessing client business opportunity, profitability, and standing; create, update, formulate and format spreadsheets; and be able to maintain client project P&amp;Ls.</li><li>
Quotation creation, pricing development and the corresponding discussions and negotiations with clients are part of this role, with appropriate sales/manager/executive level support.</li><li>
Track and trend sales, adjust sales movement and weekly events, reporting to cross-functional team, business unit and Management. Contribute and maintain the customer database and systems within CSM II&rsquo;s responsibility.
</li><li>Ensuring that all client contracts and agreements are followed and fulfilled. Particularly around change issues, assessing fees for changes and managing current pricing.</li><li>
Ability to define problems, collect data, establish facts, and draw valid conclusions impacting profitability and inefficiency, while expressing them in both writing and a professional dialogue.</li><li>
Navigate and optimize the proposal and quote process, including taking part in development of pricing study to expedite the optimal work product for delivery to client.</li><li>
Other duties may be assigned.
</li></ul></li></ul></li></ul>Essential Skills and Qualifications:<ul><li>
Bachelor's degree in a relevant field (e.g., Business, Life Sciences, Healthcare) or equivalent.</li><li>
Minimum of 5 years of experience in a client-facing role within a CDMO.</li><li>
Experience in product management, project management, client services, or sales is highly preferred.</li><li>
Experience in a Contract Development and Manufacturing Organization (CDMO) or Contract Manufacturing Organization (CMO) is REQUIRED.</li><li>
Excellent written and verbal communication skills in English.</li><li>
Ability to effectively present information to diverse audiences (clients, colleagues, leadership).</li><li>
Strong analytical and problem-solving skills with the ability to analyze data and draw conclusions.</li><li>
Understanding of basic financial concepts (e.g., gross margin, overhead).</li><li>
Ability to analyze complex situations, identify root causes, and develop effective solutions.</li><li>
Strong decision-making and problem-solving skills.</li><li>
Ability to think critically and strategically.</li><li>
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook).</li><li>
Experience with CRM systems, project management software, and other relevant business applications.</li><li>
While this role does not have direct supervisory responsibilities, it may involve coaching and mentoring junior team members (CSM I, CS Support Specialists) on client service processes and best practices.</li></ul>
Work Environment:
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. The noise level in the work environment is usually moderate.
Physical Demands:
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job the employee is regularly required to sit; use hands to finger, handle, or feel and talk or hear. The employee is occasionally required to reach with hands and arms. The vision requirements include close vision for heavy computer use.
The above job description is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow any other instructions, and perform any other related duties, as assigned by their supervisor.</div>

Client Services Manager II

Sunrise Research Institute

About 3Sync Research3Sync Research is a growing clinical research organization dedicated to advancing medicine through high-quality clinical trials. We partner with leading pharmaceutical companies, CROs, physicians, and healthcare professionals to bring innovative treatment options to diverse patient populations.Our office conducts outpatient clinical research across multiple therapeutic areas, including primary care, pediatrics, asthma/allergy, diabetes, endocrinology, infectious disease, vaccines, and other adult and pediatric studies. We are looking for a strong, experienced provider who is comfortable working directly with patients and supporting clinical trial oversight.Position OverviewWe are seeking a bilingual APRN / Nurse Practitioner to join our clinical research team as a Clinical Trial Sub-Investigator. This is an excellent opportunity for an experienced provider who is detail-oriented, and comfortable working with both adults and children.In this role, you will work closely with the Principal Investigator, site directors, operations leadership, recruitment team, clinical research coordinators, sponsors, CROs, and regulatory teams to support the safe and compliant conduct of clinical trials. The Sub-Investigator will conduct patient screening, eligibility review, physical exams, safety assessments, protocol compliance, clinical documentation, enrollment support, participant retention, and contribute to overall site performance.Key ResponsibilitiesAssist the Principal Investigator in the oversight and execution of clinical trialsConduct patient screening, enrollment, and ongoing study visit assessmentsPerform physical exams and clinical evaluations for adult and pediatric participantsReview medical history, medications, labs, vitals, inclusion/exclusion criteria, and study eligibilityMonitor participant safety throughout the studyIdentify, assess, document, and report adverse events and clinical concernsPerform or assist with blood draws, vital signs, and other protocol-required proceduresReview informed consent forms, source documents, lab reports, CRFs, and study records for accuracy and completenessSupport protocol compliance, data collection, and audit readinessCommunicate professionally with participants, parents/guardians, study staff, sponsors, CROs, and regulatory teamsSupervise and support clinical research staff when neededCollaborate closely with site directors, operations leadership, recruitment teams, coordinators, and the Principal Investigator to support successful study outcomes, strong enrollment, participant retention, protocol compliance, and overall site performanceServe as a team player within a fast-paced clinical research environment, helping ensure smooth communication between clinical, operational, and recruitment staffEnsure study activities are conducted in compliance with FDA regulations, ICH-GCP guidelines, HIPAA, protocol requirements, and site SOPsRequirementsActive and unrestricted License/Certification- Florida APRN / Nurse Practitioner License requiredMinimum of 5+ years of experience as an APRN / Nurse Practitioner(Bilingual English/Spanish )Must be comfortable working with both adult and pediatric patientsStrong clinical assessment, documentation, and decision-making skillsExperience with patient evaluation, medical history review, medication review, labs, and clinical proceduresPhlebotomy or blood sampling experience preferredFamiliarity with medical terminology, clinical documentation, and outpatient patient careAbility to work independently while collaborating with the Principal Investigator and research teamStrong attention to detail and ability to work in a fast-paced clinical environmentProfessional, dependable, organized, proactive, and team-orientedGCP certification preferred; training can be provided if neededAvailability to work occasional weekends as needed based on study requirementsPreferred ExperienceFamily MedicinePrimary CarePediatricsInternal MedicineUrgent CareAllergy / AsthmaEndocrinologyDiabetes CareInfectious DiseaseVaccinesClinical ResearchClinical Trial Sub-Investigator experienceIdeal CandidateThe ideal candidate is an experienced, bilingual provider who is comfortable making clinical assessments, asking the right questions, identifying safety concerns, and working with a wide range of patients. We are looking for someone who is confident in their clinical judgment, reliable, personable, and able to take ownership of patient evaluations in a research setting.This person should also be a strong team player who works well with site directors, operations leadership, recruitment teams, coordinators, and the Principal Investigator to help drive successful study outcomes, strong enrollment, participant retention, protocol compliance, and overall site performance.Why Join 3Sync ResearchOpportunity to work on innovative clinical trials and emerging treatmentsAdult and pediatric patient populationGrowing research organization with expanding study opportunitiesCollaborative team environmentExposure to multiple therapeutic areasFlexible schedule availableMeaningful role in supporting patient safety and advancing clinical researchBenefits:Health insuranceDental insuranceVision insurancePaid time offPay: $88,117.74 - $106,120.29 per yearBenefits:<ul><li>Dental insurance</li><li>Health insurance</li><li>Paid time off</li><li>Vision insurance</li></ul>Work Location: In person

Bilingual APRN / Nurse Practitioner

Huntsville Hospital Health System

<div>Overview:
<div>
Reporting to the manager, clinical informatics, the clinical informaticist is the hospital liaison for clinical informatics to the Medical Staff, Pharmacy and other Clinical Departments. Responsibilities will include: Physician systems orientation, CPOE execution, on-boarding, training and meaningful use compliance.
</div>Qualifications:
<div>
Education: BSN required. Degree in clinical informatics or RNBC (Board Certified by the ANCC in nursing informatics) preferred.</div><div>
License: Alabama Board of Nursing RN Degree &ndash; preferred. Current RNBC if no degree in clinical informatics, preferred.</div><div>
Experience: Clinical work practice, Clinical Information Systems implementation, oversight or programming, Other positions requiring Medical Staff relationships and project development. Management experience.</div></div>

Clinical Informatics Specialist-Technical Services-FT-1st shift

Piper Companies

<div>
 
 Piper Companies
 
 is looking for an
 
 In-House Clinical Research Associate
 
 to join a clinical research company located in
 
 Bethesda, MD.
 
 
 
 
 Responsibilities of the In-House Clinical Research Associate include:
 
 
 
 <ul>
 <li>
 Review and process essential regulatory documents received from clinical trial sites
 </li>
 <li>
 Request missing or additional documentation and respond to protocol or process-related inquiries
 </li>
 <li>
 Maintain and organize Trial Master Files (TMF) and centralized document systems
 </li>
 <li>
 Track regulatory documents and workflow in a centralized web-based system or database
 </li>
 <li>
 Ensure documents meet FDA, ICH GCP, and sponsor requirements for accuracy and completeness
 </li>
 <li>
 Troubleshoot regulatory document issues and follow up with study sites as needed
 </li>
 <li>
 Support distribution of trial-related materials and assist with study team coordination
 </li>
 <li>
 Assist with monitoring visit preparation and follow-up, including teleconference coordination
 
 
 </li>
 </ul>
 
 Qualifications for the In-House Clinical Research Associate include:
 
 
 
 <ul>
 <li>
 3&ndash;5 years of experience in a clinical research setting
 </li>
 <li>
 Experience with regulatory document review/collection and knowledge of FDA and ICH GCP guidelines
 </li>
 <li>
 Experience with eTMF systems (e.g., Veeva Vault) and system administration skills
 </li>
 <li>
 Experience with Trial Master Files and centralized tracking systems
 </li>
 <li>
 Experience with IRB submissions and OHRP regulations is a plus
 </li>
 <li>
 Bachelor&rsquo;s degree required
 </li>
 <li>
 Strong organizational, communication, and time management skills
 </li>
 <li>
 Proficiency with Microsoft Office (Word, Excel, Outlook)
 
 
 </li>
 </ul>
 
 Compensation for In-House Clinical Research Associate includes:
 
 
 
 <ul>
 <li>
 Rate Range: $50,000&ndash;$80,000, depending on experience
 </li>
 <li>
 Comprehensive Benefit Package: Cigna Medical/Dental/Vision, 401K, Sick Leave as Required by Law
 
 
 </li>
 </ul>
 
 This job is open for applications on June 1st, 2026. Applications will be accepted at least 30 days from the posting date.
 
 
 
 Keywords: Clinical Research, Clinical Trials, Clinical Operations, In-House CRA, TMF, Trial Master File, eTMF, Veeva Vault, Regulatory Documents, Regulatory Affairs, Document Management, ICH GCP, FDA Regulations, Good Clinical Practice, Essential Documents, Site Document Collection, IRB Submissions, OHRP Regulations, Site Start-Up, Study Coordination, Clinical Study Support, Monitoring Support, TMF Maintenance, Document Tracking, Compliance, Audit Readiness, Clinical Data Management, Sponsor Oversight, CRO, Protocol Compliance, Investigator Communication, Site Management, Clinical Systems, Database Tracking, Microsoft Excel, Microsoft Word, Microsoft Outlook
 
 
</div>

In-House Clinical Research Associate

Search 2548+ Clinical dermatologist jobs near you this June. New roles added regularly across leading industries. Apply today.