Clinical Medical Writer II - Ophthalmology & Regulatory
Trident Consulting
Trident Consulting Inc. is seeking a Medical Writer II for a 6-month assignment in the United States. The role focuses on high-quality clinical and regulatory documentation, translating complex data into clear narratives, and ensuring compliance with regulatory guidelines and templates. Collaboration with cross-functional teams, preparation of CSRs and study-related documents, and careful attention to detail are essential. The position offers standard W2 pay of $42-44/hr for first shift work. #J-18808-Ljbffr Trident Consulting
- ...Medical Writer IITrident Consulting is seeking a Medical Writer II for one of our clients in Aliso Viejo, CA (Onsite).... ...for producing high-quality clinical and clinical regulatory documentation that requires... ...processes preferred.Ophthalmology experience preferred.Excellent...RegulatoryWork at office
$35.38 - $44 per hour
...Medical Writer IIEastridge Workforce Solutions is committed... ...a Medical Writer II to support our client... ....Job Summary:Prepare clinical study reports (CSRs)... ...data consistency and regulatory complianceTranslate clinical... ...and key dates for ophthalmology-related scientific...RegulatoryHourly payTemporary workWork at officeMonday to Friday- ...Position SummaryThe CDI Specialist Level II is responsible for conducting clinically based concurrent and retrospective reviews of inpatient medical records to evaluate if clinical... ...hospital policies and procedures, and all regulatory agencies, including State and Federal...RegulatoryFull timeLocal area
- ...region. The Advanced Telemetry RN at the Clinical Nurse II level is responsible for continuous... ...rhythms and neurological status, administer medications including non-titratable drips, and... ...adhering to infection control and regulatory standards such as The Joint Commission...Regulatory
- The Sr. Scientist II, Toxicology is responsible for leading and executing nonclinical... ...and safety studies that enable clinical development and regulatory submissions. The position... ...is an ophthalmic pharmaceutical and medical technology company focused on developing...RegulatoryLocal area
- Supplier Quality Engineer II (Aliso Viejo, CA)**... ...activities for medical device and pharmaceutical... ...Product Development, Regulatory Affairs, third-party logistics... ...innovation in ophthalmology and helps improve the... ...real science, robust clinical evidence, and an unrelenting...RegulatoryWork at officeLocal area
- Sr. Scientist II, Biologics, Aliso Viejo, CAWhat You’ll Do:This... ...from early-stage clinical studies through commercialization... ...technical reports in support of regulatory submissions. Independently authors... ...pharmaceutical and medical technology company focused on...RegulatoryLocal areaWorldwide
- ...ophthalmic pharmaceutical and medical technology company... ...real science, robust clinical evidence, and an... ...Scientist / Senior Scientist II, PharmacologyHow You’... ...dose selection, and regulatory submissions.The... ...awareness of advances in ophthalmology, ocular pharmacology,...RegulatoryLocal areaFlexible hours
$134.2k - $188k
About the RoleThe Manager II, Enterprise Applications (R&D & GxP Systems) is a hands-... ...systems aligned with business needs and regulatory requirements.Let’s talk about some of the... ...platforms and other validated systems supporting Clinical, Regulatory, Quality and other regulated...RegulatoryWork at officeLocal areaRemote work$70.73k - $94.3k
...for Everyone. As the Development Engineer II CONTRACTOR, you will: Responsibilities... ...connected products. Familiarity with carrier, regulatory, or industry certification processes and... ...your eligible dependents for competitive medical, dental, vision and prescription benefits...RegulatoryFull timeContract workTemporary workFor contractorsFor subcontractorWork at officeLocal areaImmediate start- ...Consulting is seeking a "Clinical Data Manager" for one... ..." a global leader in medical technology and... ...Clinical Data Manager - Ophthalmology Location: Aliso Viejo... ...Clinical Data Manager II is responsible for study... ...Managers, Programming and Regulatory. Oversee delivery...RegulatoryContract workWork experience placementRemote work
- ...Job Title: Senior Medical Editor - Pharmaceutical Advertising Location: Remote (Priority consideration for candidates near Irvine,... ...does not include tagging, linking, Veeva work, or promotional regulatory submission preparation. The ideal candidate must be comfortable...RegulatoryContract workFor contractorsFreelanceRemote workFlexible hours
$22 - $31.9 per hour
Loan Adjuster II Pay Range: $22.00 - $31.90 Scheduled Weekly Hours: 40 What You’ll Be Doing Collects on loans of all stages of delinquency... ...searches. Performs other duties as assigned. Complies with regulatory compliance and assigned training requirements including but not...RegulatoryWork at officeRemote work3 days per week- ...Description: We are seeking a Systems Engineer II to join a Device and Combination Product... ...meet applicable safety, quality, and regulatory requirements. Identify project risks and... ...within a regulated industry, particularly Medical Device, Pharmaceutical, Biotech, or...Regulatory
- Job-ID31554631Reference25-04530 Responsibilities: This position is responsible for the preparation of regulatory submissions required to market medical devices in both the U.S. and Europe, support of international product registrations and related regulatory affairs activities...RegulatoryWork at office
$108k - $153k
...can change a patient’s life. We generate extensive clinical evidence to demonstrate the effectiveness and... ...partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will drive the evidence needed...RegulatoryWork experience placementWork at office- ...compassionate, patient-centered care with advanced clinical skills. The position demands autonomy,... .... Educate patients and families on medical conditions, treatments, and lifestyle... ...adhering to infection control and regulatory standards. Follow aseptic techniques...Regulatory
$88.22k - $132.33k
...to join our exceptional team. Position: Asset Liability Analyst II Pay Range: $88,221.00 - $132,331.00 Scheduled Weekly Hours: 40 What... ...Job Functions Perform other duties as assigned. Comply with regulatory compliance and assigned training requirements, including but not...RegulatoryWork at officeRemote work3 days per week- ...treatment program. This role reviews medical history, applies screening... ...with patient to determine clinical needs, impairments,... ...accordance with professional and regulatory standards. -Participates in outside... ..., the Speech Therapist II assists with orienting new staff...Regulatory
$225k - $250k
...collaborative team with deep expertise across ophthalmology, drug delivery, pharmaceuticals, and medical devices. Our scientists, engineers, and clinical leaders bring decades of experience... ..., Medical Affairs, Commercial, and Regulatory teams to support external scientific...RegulatoryWork at officeRemote work- ...Clinical Research Associate IIJoin the forefront of groundbreaking research at the Beckman Research... ...detail-oriented Clinical Research Associate II to manage multiple research protocols with a focus on efficiency, regulatory compliance, and study oversight. In this role...RegulatoryHourly payWork experience placement
- ...units. The Advanced Telemetry RN at the Clinical Nurse II level demonstrates specialized skills... ...and overall condition. Administer medications, including non-titratable drips, and monitor... ...policies. Comply with regulatory standards such as The Joint Commission...Regulatory
- ...as they become available. Title: Electronic Services Specialist II FLSA Status: Non-Exempt Location: Corporate Office (Foothill... ...external partners to resolve issues and ensure compliance with regulatory and internal standards. The Specialist II is expected to work independently...RegulatoryWork at officeLocal areaMonday to Friday
- ...Northwest. The Advanced Telemetry RN at the Clinical Nurse II level requires specialized skills,... ...and overall condition. Administer medications, including non-titratable drips, and... ...institutional policies. Comply with regulatory standards such as The Joint Commission...Regulatory
- ...We are seeking a dedicated Wildlife Biologist II/Arborist to contribute to our environmental conservation efforts. The successful... ...practices. Collaboration with local communities, stakeholders, and regulatory agencies will be essential to ensure the effectiveness of...RegulatoryLocal area
- Sr. Quality Engineer II / Sr. Quality Specialist IIJoin a team... ...products (pharmaceutical and medical device). In this role, you’ll... ...and to ensure quality and regulatory compliance with 21 CFR Parts... ...Collaborate with R&D, Operations, Clinical, and Regulatory teams to...RegulatoryLocal area
- ...Title: Systems Engineer II Duration : 12 Months... ...documentation meet all safety and regulatory compliance requirement.... ...scientific discipline. Effective writer and communicator of research or... ...experience in regulated industry (like Medical Device, Pharma & Biotech)...RegulatoryFor contractors
- ...Occupational Therapist IIOccupational Therapist II – Full-Time Join the transformative team... ...its Los Angeles campus, a network of clinical care locations across Southern California... ...therapy techniques, in alignment with regulatory standards and the philosophy of City of Hope...RegulatoryFull timeInternship
$141.97k - $156.55k
...of donation. Join a team of medical professionals who use skills... ...Transplant Coordinator (PTC‑II), you will provide primary medical... ...Coordinator (PTC‑II) is the clinical professional responsible for... ..., training, and regulatory duties. Duties And Responsibilities...RegulatoryFull timeWork at officeShift workNight shift- ...professional to support product data process development for medical devices, creating and maintaining digital product processes, validating... ...-of-life. You will collaborate with Operations, R&D, Quality, Regulatory and IT to optimize engineering processes, perform validation,...Regulatory
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