Medical Writer II: Clinical, Regulatory & CER Expert
Laborie Medical Technologies Corp.
Laborie Medical Technologies Corp. is seeking a Medical Writer II in Minnetonka, Minnesota. The role involves developing clinical, scientific, and regulatory documents while collaborating with internal and external partners to support technical writing functions. Qualified candidates will have a Bachelor's degree in a relevant scientific or writing field and at least 5 years of experience in medical writing. The position offers comprehensive benefits including paid time off, health insurance, and a retirement plan with company match. #J-18808-Ljbffr
- Laborie Medical Technologies Corp in Minnetonka, MN is seeking a Medical Writer II to develop clinical and regulatory documents and presentations. This role involves collaboration with internal and external partners to support technical writing functions for Clinical and...Regulatory
- ...with Passion. Who We’re Looking For: The Medical Writer II collaborates in the development and execution of clinical, scientific, and regulatory documents and presentations for internal... ..., and clinical evaluation reports (CERs) and Clinical Study Reports (CSRs). Search...RegulatoryFlexible hoursShift work
$78k - $156k
Senior Medical Writer, Clinical Evaluation (on-site) page is loaded## Senior Medical Writer, Clinical... ...Evaluation**. The Sr. Medical Writer on our Regulatory Clinical Evaluation team provides... ...in planning for and supporting CER related projects and processes.* Supports...RegulatoryWork experience placement- ...Synergy Ablation System is the first medical device to receive FDA approval for... ...and personally. Position Summary The Clinical Research Associate II (CRA II) at AtriCure is a critical role... ...compliance with study protocols and regulatory standards. The CRA II plays a...RegulatoryTemporary workInterim roleWork at officeLocal areaWorldwide
$66.8k - $120k
...Office Job Description Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront... ...site visits to assess protocol and regulatory compliance and manage required documentation... ...Demonstrated understanding of medical/therapeutic area knowledge and...RegulatoryTemporary workWork at officeRemote workHome officeFlexible hoursNight shift- ...Stryker Corporation is seeking a Coder II in Eden Prairie, Minnesota to assign ICD-10-CM/PCS codes for inpatient encounters, ensuring compliance with coding guidelines. This role supports accurate reimbursement and data integrity for Powers Health hospitals. Applicants...Remote work
- A global healthcare leader is seeking a Senior Medical Writer for its Maple Grove, MN location. The role involves writing Clinical Evaluation Reports, collaborating across departments, and ensuring compliance with regulations. Candidates should have a Bachelor's degree...
- ...inVentiv Health Commercial LLC is seeking a Sr Medical Writer Publications to lead the completion of medical writing deliverables across clinical studies. The ideal candidate will ensure... ...is clear and accurate while adhering to regulatory standards. Responsibilities include...RegulatoryRemote workFlexible hours
- ...Summary We are currently seeking a PSC Ambulatory II-FOH to join our Psychiatry Clinic team. This 0.70 (56 hours per pay period) role will primarily... ...Clinical leadership Leads and functions as the Subject Matter Expert (SME) in assigned areas Assist with facilitation daily...Work at officeShift workWeekend workDay shiftAfternoon shift
- ...Rotations Required ***Will Consider Clinical Laboratory Scientist I, II or III*** Position Summary:... ...experience, the Clinical Lab Scientist 3 (Medical Technologist or Medical Lab... ...operating procedures, policies and regulatory guidelines. These require a professional...RegulatoryFull timeWork experience placementInternshipWeekend work
$72.8k - $130k
Optum is seeking a Clinical Documentation Integrity (CDI) Specialist in Eden Prairie, Minnesota. This hybrid position will involve performing... ...reviews, maintaining coding knowledge, and collaborating with medical providers for documentation improvement. Candidates should have...- ...AtriCure, Inc. in Minnetonka, Minnesota is seeking a Senior Clinical Research Associate (Sr. CRA) to independently manage and oversee... ...involves coordinating site communications, ensuring compliance with regulatory standards, and mentoring junior team members. A bachelor's...Regulatory
$78.7k - $118.02k
Medica Services Company LLC in Minnetonka is seeking a Clinical Regulatory Oversight Business Analyst III to provide analytical documentation... ...a generous total rewards package including competitive medical, dental, vision benefits, and more. #J-18808-Ljbffr Medica...RegulatoryWork at office3 days per week- ...and directs Applied Behavior Analysis (ABA) programs, providing clinical supervision to behavior technicians and ensuring high-quality... ...stakeholders Ensure compliance with ethical guidelines and regulatory requirements Participate in treatment team meetings and...Regulatory
- A leading medical device company is seeking a Post-Market Clinical Affairs Specialist to ensure regulatory compliance and the safe use of dental products. Responsibilities include leading PMCF activities, providing expertise in clinical evaluations, and developing clinical...RegulatoryRemote job
$100.3k - $150.47k
Medica in Hopkins, MN is seeking a Clinical Regulatory Oversight Program Manager to oversee compliance with federal, state, and accreditation requirements affecting Clinical Services. The role demands expertise in regulatory consultation and vendor oversight, ensuring policies...RegulatoryWork at office$86.4k - $129.6k
...A Day in the Life The Clinical Research Monitor oversees clinical... ...sites, ensuring compliance with regulatory standards, IRB/EC policies,... ...expedite clinical studies. Reviews medical records with investigators,... ...medical device and/or phase II, III, and IV pharmaceutical...RegulatoryTemporary workH1bRemote workFlexible hoursShift work$80k - $105k
...Health Center Lead II, RN The Health Center Lead II, RN will... ...dual-function role blends clinical insight with operational oversight... ...of Operations, Market Medical Director, and others to align... ..., scheduling, inventory, and regulatory compliance. Coordinate with...RegulatoryHourly payLive in$61.3k - $122.7k
Quality Engineer II The Opportunity This position works out of our Minnetonka, MN location... ...of heart disease through breakthrough medical technologies in atrial fibrillation,... ...Environmental Management Systems (EMS), and other regulatory requirements. Complies with U.S. Food...RegulatoryWork experience placementAfternoon shift$106k - $145.75k
Post-Market Clinical Affairs Specialist As a Post-Market Clinical Affairs Specialist, you... ...with diverse teams worldwide to ensure regulatory compliance and support the safe, effective... ...of three (3) years of experience in the medical device industry. Minimum of three (3)...RegulatoryH1bWork at officeRemote workWorldwideRelocation packageFlexible hours- ...Senior Clinical Research Associate We believe that great healthcare... ...a critical role in advancing medical devices from concept through... ...evidence generation to meet regulatory and commercialization needs.... ...documentation (e.g., PMS, PMCF, CER, CEP), as needed. What you...RegulatoryLocal area
$85k - $104k
...Synergy Ablation System is the first medical device to receive FDA approval for... ...personally. POSITION SUMMARY: The Clinical Research Associate II (CRA II) will be a key contributor... ...protocol, SOPs, GCP, and applicable regulatory requirements to the investigator and...RegulatoryTemporary workInterim roleWork at officeLocal areaRemote workWorldwide- ...JOB DETAILS Department: CSC Urology Clinic FTE: 1.00 (80 hours per pay period) Workdays:... ...Lead and functions as the Subject Matter Expert (SME) in assigned areas Assist with facilitation... ...Certification Solid understanding of medical terminology Solid understanding of payer/...Work at officeMonday to FridayShift workWeekend workDay shiftAfternoon shift
$78.7k - $134.9k
...A nonprofit health plan is looking for a Supervisor of Quality Reviewers to oversee clinical reviews and regulatory audit operations. The ideal candidate will have a Bachelor's degree, significant clinical healthcare experience, and leadership skills. This role includes...Regulatory$100.3k - $172k
The Clinical Regulatory Oversight Program Manager is responsible for supporting the operational implementation... ...a clinical regulatory subject matter expert, ensuring policies, procedures,... ...total rewards package that includes medical, dental, vision, paid time off, holidays...RegulatoryWork experience placementWork at office3 days per week- ...For: Under the guidance of Clinical Affairs leadership, the... ...appropriate device claims and regulatory required clinical documentation... ...documentation (e.g., PMS, PMCF, CER, CEP) as needed and support... ...Medicine, Nursing or related medical discipline with 8 years relevant...RegulatoryTemporary workFlexible hours
- ...A leading medical technology company is seeking a Software Design Assurance Engineer II based in Eden Prairie, Minnesota. This role involves supporting design assurance... ...for medical devices, ensuring compliance with regulatory standards, and leading risk management...Regulatory
- ...A healthcare organization in Minnesota is seeking a Clinical Research Coordinator to oversee patient care in clinical research studies, ensuring compliance with protocols and regulatory standards. The ideal candidate will have a nursing degree and experience in clinical...Regulatory
$107k - $170k
...Philips Iberica SAU is looking for a Senior Clinical Research Associate responsible for ensuring adherence to clinical study protocols and regulatory requirements in Plymouth, Minnesota. Candidates should have a strong background in clinical research, especially in FDA...Regulatory$60.7k - $106k
...team, the Senior Technical Writer role for Medi-Span is responsible... ...of embedded drug data and Clinical Decision Support solutions.... ...Support relevant healthcare regulatory requirements (e.g., HIPAA, FDA guidelines, CE Mark/Medical Device Regulation). Follow industry...RegulatoryWork at officeRemote work
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