Safety Writer Ii

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through...

**Job ID: ABOJP00037257** **Job Title: Medical Writer II** **Duration: 11/15/2024 to 06/30/2025** **Location: Abbott Park** **IL- 60064 (Remote)** **Remote 20 to 30 hour a week flexibility** **structural heart division** - **Publication or portfolio link must be designated on the resume.**: - Prepare technical document support clinical and medical...

Summarized Purpose: Responsible for the planning, coordination and delivery of safety writing services for multiple clinical trial and/or marketed product projects. Performs day-to-day safety writing and related activities within a highly regulated pharmacovigilance environment, driven by strict timelines. Activities include but are not limited to delivery...

**Job Purpose**: - Responsible for management of scheduled and unscheduled aggregate reports including but not limited to Periodic Safety Reports (PSRs) including Periodic Safety Update Reports (PSURs), Periodic Benefit-Risk Evaluation Reports (PBRERs), Addendum to Clinical Overviews (ACOs), Semi-Annual Safety Reports (SASRs), Corporate Addendum Reports,...

Safety Scientist II - (client embedded) - At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals...

As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. **Responsibilities**: The Clinical Research Associate is ultimately responsible for the successful management of investigator sites throughout the trial lifecycle. Key responsibilities include: - Full ownership of...

As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.**Responsibilities**: - The Clinical Research Associate is ultimately responsible for the successful management of investigator sites - throughout the trial lifecycle. Key responsibilities include: - Full ownership of...

**Description** **Central Monitor II** Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the...

Company Description Zayo provides mission-critical bandwidth to the world’s most impactful companies, fueling the innovations that are transforming our society. Zayo’s 141,000-mile network in North America and Europe includes extensive metro connectivity to thousands of buildings and data centers. Zayo’s communications infrastructure solutions include...

**Description** **Principal Safety & Pharmacovigilance Specialist** Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide...

**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office Summarized Purpose: We are looking for a CTC I / II - FSP to join our team at Thermo Fisher Scientific Inc. This role offers an excellent chance for someone ambitious to make a significant impact on the future of clinical trials. Your work will focus on flawlessly executing clinical...

**Description** **Principal Medical Writer** Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide practical value to help our...

**Job Purpose**: - Responsible for management of scheduled and unscheduled aggregate reports including but not limited to Periodic Safety Reports (PSRs) including Periodic Safety Update Reports (PSURs), Periodic Benefit-Risk Evaluation Reports (PBRERs), Addendum to Clinical Overviews (ACOs), Semi-Annual Safety Reports (SASRs), Corporate Addendum Reports,...

Key Responsibilities:Procure and stock assigned kitchen facilities with raw materials and ingredients on a daily basis.Familiarize yourself with the operation and maintenance of all electrical and mechanical equipment in the kitchen, adhering to safety protocols.Work Environment:Full-time employment with AccorHotel.Remote Work:No

**Freelance Content Creator - OSHA Training** **Position**: Freelance Content Creator - OSHA Training **Location**: Remote **Duration**: Project-Based **About Us**: **Key Responsibilities**: - **Content Creation**: Develop clear, engaging, and informative OSHA training content, including scripts, video narrations, quizzes. - **Research & Compliance**:...

**Description** **Medical Writer I** Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the...

**Summarized Purpose**: Performs advanced aspects of the data cleaning process with a high level of accuracy and in accordance with GCPs and SOPs/WPDs, to assess the safety and efficacy of investigational products and/or medical devices.**Essential Function**: ** Identifies, resolves, and updates data discrepancies. Makes changes to the data management...

India, Remote **Additional Locations**: Hyderabad, Telangana, India **Job ID** R0000028190 **Category** Data Management **ABOUT THIS ROLE**: **Job Purpose** **Set-Up Database**: - Create, implement and execute procedures to build and maintain database set-up for paper based and/or web based (EDC) clinical data management systems (CDMS) in standard...

Why Patients Need You Pfizer Worldwide Medical and Safety colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes. Whether you are creating framework necessary to ensure our evidence is scientifically sound, providing unbiased, medically necessary...

As a Statistical programmer (all level) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Working Location: India, Home-based We are the global biostatistics team dedicated to late phase research, working on (but not limited to) peri and post approval research, post...