8 Abstracts Jobs

As a Consultant / Sr. Consultant - Scientific Writer, your role involves preparing literature reviews, abstracts, posters, slide sets, and manuscripts (complex) by working with various data sources such as clinical study reports and patient profiles. You are responsible for performing quality control (QC) checks and proofreading of the deliverables to ensure they meet customer expectations. It is essential for you to comply with and support the group's project management tools, standards, policies, and initiatives. Maintaining records for all assigned projects, including archiving, and ensuring audit, SOP, and training compliance are also key responsibilities. - Prepare literature reviews, a...

Description Medical Writer II (Narrative Writing) 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 center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem s...

As a Clinical Associate in the department of Radiology & Imaging at Tata Medical Center, Kolkata, your role will involve the following responsibilities: - Engage in reporting CT / MRI / X-ray and USG scans. - Perform Intervention procedures both in Cath lab and guided settings. - Take part in and lead departmental audits, quality assurance, and educational activities. - Participate in departmental research, publications, and abstracts. - Engage in teaching DNB students in radiology, Fellowship Programme in Onco Radio Imaging and Interventions, and DRD students. Qualifications required for this position include: - MD/DNB in Radiology and Imaging. Experience: - At least 2 years of experience p...

The role of Consultant / Sr. Consultant - Scientific Writer involves preparing literature reviews, abstracts, posters, slide sets, and manuscripts (complex) by working with various data sources such as clinical study reports and patient profiles. You will be responsible for performing quality control (QC) checks and proofreading of the deliverables to ensure they meet customer expectations. It is essential to comply with and support the group's project management tools, standards, policies, and initiatives. Maintaining records for all assigned projects, including archiving, and ensuring audit, SOP, and training compliance are also key responsibilities. The ideal candidate should have experti...

ZS is a place where passion changes lives. As a management consulting and technology firm focused on improving life and how we live it, our most valuable asset is our people. Here you'll work side-by-side with a powerful collective of thinkers and experts shaping life-changing solutions for patients, caregivers, and consumers, worldwide. ZSers drive impact by bringing a client-first mentality to each and every engagement. We partner collaboratively with our clients to develop custom solutions and technology products that create value and deliver company results across critical areas of their business. Bring your curiosity for learning; bold ideas; courage and passion to drive life-changing i...

As a Medical Writer II specializing in QC of Regulatory Documents at Syneos Health, you will be responsible for compiling, writing, editing, and coordinating medical writing deliverables that present scientific information clearly and accurately. Your role will involve working within and across departments with minimal or moderate supervision to complete a variety of documents such as clinical study protocols, clinical study reports, patient narratives, investigator brochures, and more. You will adhere to established regulatory standards, including ICH E3 guidelines and company standard operating procedures, while completing medical writing projects on time and within budget. Additionally, y...

You will be responsible for writing, supporting, and managing projects to create high-quality medical and scientific communications, such as literature reviews, abstracts, posters, slide sets, and complex manuscripts for publication or presentation at congresses or to internal medical and clinical teams. You will work from various data sources, including clinical study reports and patient profiles, to prepare these deliverables. Additionally, you will perform quality control checks and proofreading to ensure the final outputs meet customer expectations. You will manage multiple projects simultaneously, focusing on up to two brands at a time. Gathering feedback from customers and implementing...

The job involves preparing literature review, abstracts, posters, slide sets, and manuscripts from various data sources such as clinical study reports and patient profiles. Quality control and proofreading of deliverables are essential to meet customer expectations. Adherence to project management tools, standards, policies, and initiatives is required. Record-keeping for projects and compliance with auditing, SOP, and training are key responsibilities. The role is for a Consultant / Sr. Consultant - Scientific Writer in the Pharmaceutical industry. It is a full-time, permanent position in the outsourcing/Offshoring category. The key skills include literature review, abstracts, posters, slid...