Medical Writer Systimmune IncMedical WriterPrinceton, NJ$80,000–$130,000 / yearPosition Summary: The medical writer will be responsible for the management and oversight of assigned medical writing projects, including clinical study protocols and reports, investigational new drug applications (INDs), investigator brochures, reviewing informed consent forms and regulatory briefing materials. Key Responsibilities: Write, edit and/or manage the production of high-quality clinical documentation including clinical study protocols, synopses, and clinical study reports for submission to regulatory authorities in support of marketing applications and BLAs.
Senior Medical Writer fingerpaintSenior Medical WriterObjectives of This Role: A Senior Medical Writer is responsible for the planning, preparation, development, and/or review of scientific/medical content in a variety of formats (slides, newsletters, storyboards, etc.); accurate interpretation of data; clear communication with clients, speakers, and HCPs; efficient planning and organization; establishing effective working interactions with account services, editorial, creative, and project management teams; and efficiently producing high-quality deliverables. Fingerpaint Group’s medical communications solutions, Fingerpaint Medical, help pharmaceutical and biotech companies communicate complex scientific data effectively, enabling healthcare providers to make informed decisions that advance patient care.
Medical Content Writer Ova TechnologiesMedical Content WriterAlpharetta, GARemoteJoin our growing healthcare content team as a Medical Content Writer , where you will create accurate, engaging, and evidence-based medical content for healthcare professionals, patients, pharmaceutical companies, and digital healthcare platforms. The ideal candidate possesses excellent writing skills, a strong understanding of medical terminology, and the ability to translate complex scientific concepts into clear, reader-friendly content.
Principal Medical Writer ICON PlcPrincipal Medical WriterBlue Bell, PAAs a Principal Medical Writer at ICON, you will be responsible for leading the development of high-quality regulatory and clinical documents that effectively communicate scientific and medical information. Collaborating with cross-functional teams, including clinical research, biostatistics, and regulatory affairs, to gather and synthesize information for document development.
Clinical Medical Writer Consultant KaztronixClinical Medical Writer ConsultantSan Diego, CARemoteThis role requires close partnership with Clinical Development, Clinical Operations, Biostatistics, Data Management, Regulatory Affairs, Pharmacovigilance, and external vendors to ensure timely delivery of accurate, scientifically rigorous documents. This individual will play a key role in advancing multiple late-stage clinical programs, with primary responsibility for authoring and coordinating clinical study documentation for Phase 2 and Phase 3 trials.
Medical Writer PhD Cardiovascular/Metabolic Cincinnati Medpace Holdings IncMedical Writer PhD Cardiovascular/Metabolic CincinnatiCincinnati, OHPhD in Life Sciences with a focus in Cardiovascular and/or Metabolic research (clinical or nonclinical);• Ability to synthesize complex information into a clear and concise format that is appropriate for the target audience;• Energetic and enthusiastic team-player that is self-motivated and eager to learn and grow in the position; and• Prior experience in the CRO, pharmaceutical, or medical writing industries is not required but is advantageous. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective.
Medical Writer PhD Hematology/Oncology Cincinnati Medpace Holdings IncMedical Writer PhD Hematology/Oncology CincinnatiCincinnati, OHPhD in Life Sciences with a focus in Hematology and/or Oncology research (clinical or nonclinical);• Ability to synthesize complex information into a clear and concise format that is appropriate for the target audience;• Energetic and enthusiastic team-player that is self-motivated and eager to learn and grow in the position; and• Prior experience in the CRO, pharmaceutical, or medical writing industries is not required but is advantageous. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective.
Senior Regulatory Medical Writer, Client-embedded, FSP Thermo Fisher Scientific IncSenior Regulatory Medical Writer, Client-embedded, FSPFramingham, MA$110,000–$125,000 / yearAs one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation, and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation, and support patients in need. The successful candidate will have a proven track record in authoring clinical regulatory documents; ideally they will also bring the versatility to author and support preclinical regulatory documents as part of a broader regulatory writing portfolio.
Assistant Medical Writer - Hybrid Role AdMed Inc.Assistant Medical Writer - Hybrid RolePhiladelphia, PAAdMed is an award winning, integrated agency that designs and delivers modern training tools for pharmaceutical, biotech, diagnostic and medical products, with one goal: to ensure that healthcare professionals, sales teams, employees and consumers understand what they need to know regarding the science behind their products. AdMed has over 30 years of industry experience and we are looking for a dynamic, passionate, experienced Assistant Medical Writer to join our team.
Contract Medical Writer (Scientific Communications) MJH Life SciencesContract Medical Writer (Scientific Communications)RemoteThis role partners with Medical Affairs and account teams to create advisory board content, training resources, and scientific messaging that supports healthcare professionals across live, digital, and field-facing channels. We are seeking a Contract Medical Writer (Scientific Communications) to support the development of high-quality, evidence-based medical communications materials.
Senior Medical Writer Nucleus Global LtdSenior Medical WriterYardley, PADrawn together from several backgrounds including the pharmaceutical industry, research, marketing, medical and regulatory writing, sales, publishing, digital media and design, we have the experience and all-round ability to conceive and deliver the best quality medical communications programs. We consider compensation more than just a base salary - that's why we also offer an exceptional range of flexible benefits, personal support and tailored learning and development opportunities all designed to help you realize your full potential both in life and at work.
Medical Writer - India (56829) Praxis Precision MedicinesMedical Writer - India (56829)Boston, MACollaborates with cross-functional team members, eg, Clinical Pharmacology, Toxicology, Research, Clinical Development, Regulatory Affairs, Biostats, Data Management, Quality, CMC, QC, etc., to ensure accurate and timely completion and delivery of high-quality, scientifically-sound documents, slide decks, and publications. This requires the knowledge and expertise to collaboratively author required documents with support and input from the Associate Director, Medical Writing while also helping other teams follow medical writing processes and style requirements.
Senior Regulatory Medical Writer - Fractional (Remote) Penfield Search PartnersSenior Regulatory Medical Writer - Fractional (Remote)Fairfield, CTRemoteSupport preparation and maintenance of protocol amendments, submission support documents, and related deliverables within Common Technical Document (CTD Modules 2–5) across the submission lifecycle (responses, amendments, briefing packages). This role focuses on independently updating and finalizing regulatory documents to support ongoing agency interactions and submission deliverables, working alongside internal and contract writers.
Senior Medical Writer Centessa Pharmaceuticals PlcSenior Medical WriterBoston, MA$150,000–$190,000 / yearOversee document preparation from start to finish, including kick-off activities and planning, drafting, managing review cycles, incorporating feedback and revisions, addressing quality control and quality assurance findings, and providing a final version within document timelines. Strong organizational, communication, and influencing skills; ability to prioritize, multitask, and deliver high-quality documents under tight timelines.
Principal Medical Writer- MedPubs Focus Synchrogenix Information StrategiesPrincipal Medical Writer- MedPubs FocusMassachusettsFinal salary is ultimately decided upon taking into account a wide range of factors, including but not limited to: skills and experience, licensure and certifications, education, specific location and dynamic market data. Proficient in MS Office Suite (advanced MS Word, PowerPoint and Excel); Adobe Acrobat for developing and editing poster slides, pdf poster layouts and slide sets.
Medical Writer CollateMedical WriterSan Francisco, CaliforniaThe base salary range for this role is competitive, depending on experience and level (Tier 1, San Francisco) We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. Serve as a pharma insider resource — helping us understand org structures, roles, timelines, and internal processes at target pharma companies, and weighing in on industry relationships and positioning (e.g., which pharma leaders and functions we should be building relationships with).
NewSenior Medical Writer Syneos - Commercial - ProdSenior Medical WriterRemote, RemoteRemote$110,000–$115,000 / yearThe Sr Medical Writer is often involved in projects from their inception, working with other Syneos Learning Solutions team members (Solution Implementation Managers, Learning Strategists, Learning Advisors, and others) to provide input into training roadmaps and timelines and attending both internal and external status meetings. Work collaboratively with team of medical writers, other team members, and clients to prepare training for sales representatives, medical science liaisons, and other professionals in the pharmaceutical and/or biotech field.
Associate Director, Medical Writer Celldex Therapeutics IncAssociate Director, Medical WriterNew Haven, CT$153,616–$199,501 / yearResponsible for the generation of clinical regulatory documents including, but not limited to: briefing documents, IND annual reports, Investigator''s Brochures, clinical protocols and amendments, clinical study reports, scientific manuscripts and abstracts. The Associate Director, Medical Writer at Celldex will lead the development and management of complex clinical and regulatory documents, including protocols, investigator brochures, study reports, and regulatory submissions for our immunology programs.
Medical Writer Nucleus Global LtdMedical WriterYardley, PARegardless of past practice, all resumes submitted by search firms to any employee of Nucleus Global and its affiliated companies via email, the Internet or in any form - without a current signed fee agreement for that position (as authorized by the Recruitment Manager) - will be deemed the sole property of Nucleus Global, and no fee will be paid in the event the candidate is hired as a result of the referral or through other means. You will be required to participate in client meetings / teleconferences and attend scientific meetings such as congress, symposia and advisory boards and participate in pre-meetings, onsite activities and post meeting work as required / appropriate.
Principal Medical Writer, Cardio/Metabolic Health ProPharma GroupPrincipal Medical Writer, Cardio/Metabolic HealthChicago, IllinoisWith deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs. For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies.
NewSr. / Principal Medical Writer (Regulatory focus) - Sponsor-dedicated; NA/CAN/UK Syneos Health IncSr. / Principal Medical Writer (Regulatory focus) - Sponsor-dedicated; NA/CAN/UKMorrisville, NCTogether we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. Selecting us as an employer secures a career in which you're guaranteed to: Collaborate with passionate problem solvers Partner with the most diverse team of experts in the industry.
Senior Medical Writer Syneos Health IncSenior Medical WriterCATogether we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. Selecting us as an employer secures a career in which you're guaranteed to: Collaborate with passionate problem solvers Partner with the most diverse team of experts in the industry.
Principal Medical Writer-nonclinical focus Synchrogenix Information StrategiesPrincipal Medical Writer-nonclinical focusMassachusettsPossesses broad experience and technical expertise across more than one therapy area and integrate this knowledge to deliver business successes and actively transfer this knowledge to strength the skill base across the organization. Final salary is ultimately decided upon taking into account a wide range of factors, including but not limited to: skills and experience, licensure and certifications, education, specific location and dynamic market data.
NewSenior Medical Writer Medtronic PlcSenior Medical WriterNorth Haven, CTRemoteThe following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program). If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
NewSenior Medical Writer MedtronicSenior Medical WriterNorth Haven, ConnecticutRemoteThe following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program). If you are applying to perform work for Medtronic, Inc. (“Medtronic”) in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
Senior Medical Writer St. Jude Children's Research Hospital IncSenior Medical WriterMemphis, TN$78,000–$139,360 / yearThis role serves not only as a key contributor to content development but also as a central project facilitator-driving cross-functional alignment, ensuring timely execution, and coordinating activities across stakeholders to support successful delivery of clinical and CMC documentation for clinical programs. CMC Medical Writer is responsible for providing clinical, scientific, technical writing, and project coordination expertise for essential clinical and chemistry, manufacturing, and controls (CMC) documents submitted to the FDA and other regulatory agencies to support St.
Medical Writer Knowesis, Inc.Medical WriterEast Orange, NJ$85,000–$89,000 / yearDevelop, write, and edit a wide range of clinical, scientific, and research-based documents, including study protocols, leadership reports, manuscripts for publication, regulatory submissions, grant proposals, and other technical materials essential to research and clinical operations. Maintain up-to-date VHA-required training for all personnel involved in patient care and/or research studies, including but not limited to: VA Privacy and Information Security Awareness and Rules of Behavior; VHA Privacy Policy Web Training; and Collaborative Institutional Training Initiative (CITI) Program Training.
Senior Medical Writer Precision Medicine Group LLCSenior Medical WriterNY$100,600–$182,600 / yearEssential functions of the job include but are not limited to: Planning, writing, editing, formatting, and QC review of timely and high-quality clinical documents including clinical study protocols, IBs, ICF templates, DSURs, CSRs, CSR patient narratives with a clear understanding of content requirements based on regulatory guidances. This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs.
Principal Medical Writer MJH Healthcare Holdings LLCPrincipal Medical WriterRemote$95,000–$105,000 / yearYou actively use tools such as ChatGPT, Claude, or AI-assisted research and writing platforms to improve how you work and can clearly articulate how they enhance output quality and efficiency - while maintaining scientific integrity and compliance. Provide mentorship, training, and editorial guidance to junior Medical Writers and Editors, supporting their development and helping the team consistently deliver high-quality work.
NewMedical Writer Position Integrated Resources, IncMedical Writer PositionGroton, ConnecticutContractorHighly organized, ability to prepare technical reports, summaries, protocols, and quantitative analysesTechnical Knowledge:Able to work well in cross-functional teams, exhibiting a combination of active listening skills and also the confidence to guide decision-making for the document content strategy. Job DescriptionResponsibilities:Prepare the Clinical Overview, integrated safety, efficacy, pharmacology and bio therapeutic summaries, regulatory responses, internal and external risk/benefit briefing documents, for one or more assigned products.
Medical Writer - PhD - Hematology/Oncology - Cincinnati Medpace, Inc.Medical Writer - PhD - Hematology/Oncology - CincinnatiCincinnati, OhioQualifications: • PhD in Life Sciences with a focus in Hematology and/or Oncology research (clinical or nonclinical); • Ability to synthesize complex information into a clear and concise format that is appropriate for the target audience; • Energetic and enthusiastic team-player that is self-motivated and eager to learn and grow in the position; and. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective.
Medical Writer - PhD - Cardiovascular/Metabolic - Cincinnati Medpace, Inc.Medical Writer - PhD - Cardiovascular/Metabolic - CincinnatiCincinnati, OhioQualifications: • PhD in Life Sciences with a focus in Cardiovascular and/or Metabolic research (clinical or nonclinical); • Ability to synthesize complex information into a clear and concise format that is appropriate for the target audience; • Energetic and enthusiastic team-player that is self-motivated and eager to learn and grow in the position; and. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective.
Medical Writer WebMD Health CorpMedical WriterNY$82,500–$90,000 / yearMedscape, a division of WebMD, develops and hosts physician portals and related mobile applications that make it easier for physicians and healthcare professionals to access clinical reference sources, stay abreast of the latest clinical information, learn about new treatment options, earn continuing medical education credits and communicate with peers. An advanced degree in a medical or science-related specialty (MD, PharmD, RN, NP, PA, PhD) is preferred; minimum of a Bachelor of Science degree (life sciences, public health, or clinical sciences) or similar with several years' relevant work experience required.
NewMedical Writer, Scientific Intelligence Vaniam GroupMedical Writer, Scientific IntelligenceRemoteA Day in the Life Deliverables Develop high-quality content for an array of projects, including publications (eg, abstracts, presentations, and manuscripts), advisory boards, scientific platforms, gap analyses, literature summaries, slide sets, and training materials. Actively contribute to the ongoing improvement of Vaniam Group’s LLM by applying and sharing deep scientific and therapeutic area expertise to inform, validate, and refine AI outputs.
Senior Medical Writer Health InteractionsSenior Medical WriterYardley, PADrawn together from several backgrounds including the pharmaceutical industry, research, marketing, medical and regulatory writing, sales, publishing, digital media and design, we have the experience and all-round ability to conceive and deliver the best quality medical communications programs. We consider compensation more than just a base salary - that's why we also offer an exceptional range of flexible benefits, personal support and tailored learning and development opportunities all designed to help you realize your full potential both in life and at work.
Associate Medical Writer MJH Life Sciences Multimedia Medical LLCAssociate Medical WriterCranbury, NJ$65,000–$75,000 / yearThe Associate Medical Writer at Pharmacy Times Continuing Education (PTCE) plays a vital role in supporting the Scientific Affairs and Business Development teams by contributing to the development of CE-certified educational content. Ability to interpret complex clinical data and outcomes reports to identify learning trends and educational needs.
Senior Medical Writer (Fixed-Term Contract) COMPASS Pathways PlcSenior Medical Writer (Fixed-Term Contract)New York, NY$135,000–$185,000 / yearCOMP360 has Breakthrough Therapy designation from the US Food and Drug Administration (FDA) and has received Innovative Licensing and Access Pathway (ILAP) designation in the UK for treatment-resistant depression (TRD) due to the pressing unmet need in this area. We are currently in phase 3 for TRD, have completed phase 2 studies for both post-traumatic stress disorder (PTSD) and anorexia nervosa and are planning a further late-stage study in PTSD.
NewMedical Writers Integrated Resources, IncMedical WritersLower Gwynedd Township, PennsylvaniaContractorMedical WritersA Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. Looking for Medical Writers in Springhouse, PAClient -Johnson and JohnsonPlease share the updated resume at sweta(at)irionline.com
Senior Medical Writer- Clinical Focus Synchrogenix Information StrategiesSenior Medical Writer- Clinical FocusMassachusettsFinal salary is ultimately decided upon taking into account a wide range of factors, including but not limited to: skills and experience, licensure and certifications, education, specific location and dynamic market data. Understand regulatory authority guidelines and requirements to be able to lead an internal project team and anticipate the effects that writing practice conventions can have on the final product when seeking health authority approval/acceptance.
Senior Medical Writer Argenx SESenior Medical WriterCA$128,000–$176,000 / yearargenx is preparing for multi-dimensional expansion to reach more patients through a rich pipeline of differentiated assets, led by VYVGART, our first-in-class neonatal Fc receptor blocker approved for the treatment of gMG, and with the potential to treat patients across dozens of severe autoimmune diseases. For the expansion of our team, argenx is looking for a Senior Medical Writer who will provide medical writing support for developing complex clinical, nonclinical, and safety documents for regulatory submissions.
Senior Medical Writer (Remote) MMSSenior Medical Writer (Remote)Baltimore, MDRemoteFull timeWrite and edit clinical development documents, including but not limited to, clinical protocols, investigator’s brochures, clinical study reports, subject consent forms, integrated safety and efficacy summaries, Module 2.7.1, 2.7.2, 2.7.3, 2.7.4, and 2.5 documents, presentation materials and publications to medical journals. Our mission is to deliver high-quality service and technology solutions – rooted in strong science and decades of regulatory experience – that will assist our clients in developing and marketing life-changing therapies to positively improve lives worldwide.
Senior Medical Writer Centessa Pharmaceuticals, LLCSenior Medical WriterBoston, MA$150,000–$180,000 / yearOversee document preparation from start to finish, including kick-off activities and planning, drafting, managing review cycles, incorporating feedback and revisions, addressing quality control and quality assurance findings, and providing a final version within document timelines. Centessa Pharmaceuticals, a wholly subsidiary of Eli Lilly and Company is advancing a portfolio of high conviction programs with strong biological validation.
Independent Contractor, Medical Writer, Publications Vaniam GroupIndependent Contractor, Medical Writer, PublicationsThe Medical Writer is responsible for developing high-quality content for an array of projects, including abstracts, presentations, manuscripts, advisory boards, scientific platforms, gap analyses, literature summaries, slide sets, and training materials. Develop high-quality content for an array of projects, including publications (eg, abstracts, presentations, and manuscripts), advisory boards, scientific platforms, gap analyses, literature summaries, slide sets, and training materials.
Medical Writer II Allen SpoldenMedical Writer IICalifornia City, CaliforniaManages the document development process from start to finish which may include generating multiple draft documents and formulating final approved versions, editing, reference retrieval, as well as managing other various processes are undergone (i.e., internal & external reviews, quality checks, audits, formatting, publishing). Participates in all necessary cross-functional document development meetings (i.e., kick-off meetings, comment resolution meetings) to ensure appropriate alignment from different stakeholders.
Medical Writer Health InteractionsMedical WriterYardley, PARegardless of past practice, all resumes submitted by search firms to any employee of Nucleus Global and its affiliated companies via email, the Internet or in any form - without a current signed fee agreement for that position (as authorized by the Recruitment Manager) - will be deemed the sole property of Nucleus Global, and no fee will be paid in the event the candidate is hired as a result of the referral or through other means. You will be required to participate in client meetings / teleconferences and attend scientific meetings such as congress, symposia and advisory boards and participate in pre-meetings, onsite activities and post meeting work as required / appropriate.
Principal Medical Writer AbbVie IncPrincipal Medical WriterChicago, ILThe Principal Medical Writer is responsible for providing scientific publications or clinical regulatory document support and advanced scientific writing expertise to the clinical teams, ensuring successful preparation of high quality submission-ready documents and effective implementation of the writing process. PK, Toxicology, eSubmissions, Regulatory, Statistical Support, Data Management, Clinical, Publishing) to ensure accurate and timely completion/delivery of information and review of scientific publications or clinical regulatory submissions.
Senior Medical Writer Lumanity IncSenior Medical WriterYardley, PARemoteWe are seeking an advanced degree life-sciences professional to serve as a Senior Medical Writer within our Medical Strategy and Communications team, which serves our clients by mobilizing our scientific knowledge to interpret the data and create compelling narratives to guide their medical strategy and through regulatory challenges. The Senior Medical Writer will ensure high-quality content is developed for a wide range of medical communications projects and deliverables including clinical publications (manuscripts and abstracts), slide decks, scientific platforms, symposia, advisory boards, and training materials.
Medical Writer III Johnson & JohnsonMedical Writer IIIPA$109,000–$174,800 / yearAll Job Posting Locations: Horsham, Pennsylvania, United States of America, Raritan, New Jersey, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America. Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.
Medical Writer Editor I ARUPMedical Writer Editor ISalt Lake City, UTPart timePrimary Purpose : Under the guidance of more senior medical writers, this position is responsible for creating technical and medical content that meets information needs related to laboratory testing. We always strive for excellence and have a strong desire to have involvement with the advances in medicine and the role laboratory services plays within each patient’s life.
NewMaintenance Technician (on-site) National Community RenaissanceMaintenance Technician (on-site)San Diego, CAMust be able to read and speak English or read and speak English and Spanish, as appropriate to the resident base, in order to effectively communicate between the Resident Services team and residents as well as between co-workers and supervisors. A minimum of 1 year or more of recent experience in property management maintenance or a related field is required while it is preferable to have 2 or more years of hands on experience.