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As a result of this success, Amiculum is looking for an experienced medical writer with a passion for publications who enjoys building positive long-term relationships, identifying opportunities, and driving organic growth. • Providing clients with a high level of scientific expertise for medical communications projects, with a focus on publications, including abstracts, posters, and manuscripts.

Amiculum

Experienced medical writer - publications - USA

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The PDM builds TULSA-PRO Clinical Programs through Champions, developing new users, driving referral pathways, and earning the hospitals commitment of resources to the TULSA-PRO program. We are changing the paradigm for treating diseases such as prostate cancer by using real-time MR Imaging, thermal ultrasound and close-loop temperature feedback control, to gently ablate the diseased tissue with minimal side effects.

Profound Medical Inc

Program Development Manager

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Effectively communicates and collaborates with Sales and Marketing, R&D, Regulatory Affairs, Library Services, Product Performance Group (PPG), Quality Engineering, Clinical Affairs, Clinical Science, Risk Management and Medical Affairs in completing clinical evaluation project related deliverables. Reviews IFUs, patient guides, Risk Management files, Clinical Evaluation Protocols, Clinical Evaluation Reports and Plans (CER/CEP), PMS Plan, PMCF Plans/Reports, SSCPs, physician training materials, ensuring alignment of risk information.

Select Source International

Medical Writer IV

With 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.

ProPharma Group Holdings LLC

Principal Medical Writer (Device)

Experience as a clinical scientist who is responsible for timely assessment of the clinical trial data and participation in safety surveillance activities for assigned studies in Phase I-III, including review of medical history, labs, vital signs, medications, and prohibited medications. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive.

Senior Medical Monitor (Remote - US)

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With 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.

ProPharma Group

You will partner on a diverse portfolio of projects spanning multiple therapeutic areas (e.g., oncology, cardiology, neurology, etc.) and collaborate with interdisciplinary teams-including research scientists, medical professionals, medical science or scientific affairs liaisons, and commercial partners-to communicate research insights. Working knowledge in one of these areas: real-world data/evidence (RWD/RWE), human genomics, clinical research concepts, computational biology (machine learning, statistics, algorithms, bioinformatics), and/or oncology.

YEAR

Tempus

Science Writer

Tempus AI Inc

FULL_TIME

Write 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 (Remote)

partner JazzHR

Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Maintains a high level of clinical expertise and professional competence by staying abreast of the latest developments, literature, and guidelines to advise on and drive current and future clinical development plans.

A career at Pfizer offers opportunity, ownership and impact. All over the world, Pfizer colleagues work together to positively impact health for everyone, everywhere. Our colleagues have the opportunity to grow and develop a career that offers both individual and company success; be part of an ownership culture that values diversity and where all colleagues are energized and engaged; and the ability to impact the health and lives of millions of people. Pfizer, a global leader in the biopharmaceutical industry, is continuously seeking top talent who are inspired by our purpose to innovate to bring therapies to patients that significantly improve their lives.

Pfizer

Senior Medical Director, Hematology

The Research Assistant will be responsible for conducting literature searches, data management, recruiting participants, obtaining consents, maintaining files, scheduling and conducting interviews of patients and family members, maintaining data collection files, assisting with data analysis and generating correspondence, reports and graphics. Analytical ability is required to prepare reports, maintain data inventory, code, transcribe interviews, develop graphs, perform literature searches, negotiate systems in several hospitals and/or human service organizations, and identify concerns/responses of participants that require termination of interview or possible intervention.

HOUR

Shirley Ryan Ability Lab

Research Assistant - Full-Time - CBM

Active, advanced Microsoft Azure certifications (e.g., Azure Database Administrator Associate, Azure Solutions Architect, or DevOps Engineer Expert).Technical Training or Professional Licensing:Active Epic Operational Database Administrator (ODBA) Certification: Must hold an active, non-expired Epic ODBA certification (Required)Epic New Version Training (NVT): Must be fully current on all Epic NVTs up to the organization''s target Epic release version to ensure they are qualified to manage and upgrade the environment immediately upon hire. Preferred QualificationsLarge Diagnostic/Lab Network Experience: 10+ years of senior-level Caché/IRIS DBA experience, with specific experience in a national reference laboratory, massive multi-tenant healthcare system, or highly integrated diagnostic network.

Quest Diagnostics Inc

Administrator, Epic Operational Database

Statistical Modeling & Machine Learning Apply advanced statistical methods and prototype predictive ML models to address healthcare challenges like patient risk stratification, readmission rates, and pharmacy supply chain optimization. You will be responsible for building robust data infrastructure to handle complex clinical and pharmacy datasets, architecting scalable data pipelines, developing predictive models, and optimizing our cloud data stack.

Info Way Solutions LLC

Senior Data & Analytics Engineer

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You will partner on a diverse portfolio of projects spanning multiple therapeutic areas (e.g., oncology, cardiology, neurology, etc.) and collaborate with interdisciplinary teams—including research scientists, medical professionals, medical science or scientific affairs liaisons, and commercial partners—to communicate research insights. Working knowledge in one of these areas: real-world data/evidence (RWD/RWE), human genomics, clinical research concepts, computational biology (machine learning, statistics, algorithms, bioinformatics), and/or oncology.

Tempus AI

Shirley Ryan AbilityLab

A minimum of 5+ years of bio-pharmaceutical industry experience in a global pharma, biotech, life science, or healthcare authority delivering medicines/therapies to a broad market across various therapeutic areas. The amount and availability of any bonus, commission,incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless anduntil paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.

AbbVie

Principal Strategic Medical Writer

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It is Siemens Healthineers' policy to comply fully and completely with all United States export control laws and regulations, including those implemented by the Department of Commerce through the Export Administration Regulations (EAR), by the Department of State through the International Traffic in Arms Regulations (ITAR), and by the Treasury Department through the Office of Foreign Assets Control (OFAC) sanctions regulations.". Be able to understand and utilize the escalation process to Sr FSR, Management, NTS, PSE, Applications Required Certifications and Training: Has completed all required VMS training classes for C3 products Has completed VMS HW Level II and Imaging Level II certification testing.

Clinical Scientist Jobs in Chicago, IL

Experienced medical writer - publications - USA Amiculum

Program Development Manager Profound Medical Inc

Medical Writer IV Select Source International

Principal Medical Writer (Device) ProPharma Group Holdings LLC

Senior Medical Monitor (Remote - US) MMS

Principal Medical Writer (Device) ProPharma Group

Science Writer Tempus

Science Writer Tempus AI Inc

Senior Medical Writer (Remote) MMS

Senior Medical Director, Hematology Pfizer

Research Assistant - Full-Time - CBM Shirley Ryan Ability Lab

Administrator, Epic Operational Database Quest Diagnostics Inc

Senior Data & Analytics Engineer Info Way Solutions LLC

Science Writer Tempus AI

Research Assistant - Full-Time - CBM Shirley Ryan AbilityLab

Principal Strategic Medical Writer AbbVie

Field Service Engineer - HW - Elgin, IL Siemens Healthineers

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