• Clinical Medical Affairs Program Manager Jobs in Washington Dc - 25365866

  • STRYKER INDIA
  • Washington Dc
  • Save Job
  • 10 - 13 Years
  • Posted : above 1 month

Job Description:

Job Snapshot Employee Type
Full-Time

Location

Washington, DC

Job Type
Clinical Affairs

Job ID
R425894

Stryker is one of the worlds leading medical technology companies and is dedicated to helping healthcare professionals perform their jobs more efficiently while enhancing patient care The Company offers a diverse array of innovative medical technologies, including reconstructive, medical and surgical, and neurotechnology and spine products to help people lead more active and more satisfying lives We are currently seeking a Clinical Medical Affairs Program Manager to join our Neurovascular Division to be in Fremont, CA or remotely anywhere in the US

Strykers Neurovascular division is focused on advancing the practice of less invasive stroke therapies through its Complete Stroke Care solutions The business is dedicated to providing innovative stroke products and services for ischemic and hemorrhagic stroke and committed to providing clinical education and support to help physicians deliver better patient outcomes Products include stent retrievers, detachable coils, stents, balloons, guidewires and microcatheters In February 2019, Stryker Corporation (NYSESYK) announced that for the ninth consecutive year has been named as one of the 2016 FORTUNE 100 Best Companies to Work For ranking 11 out of 100 If you join our organization; will be working to Make Stroke History Stroke is devastating; 1 of 20 deaths is from a stroke, according to the CDC Watch this video to see how Stryker is making a difference https//wwwyoutubecom/watchv=JANFZrpt1Hg

Who we want

Data translators Highly effective communicators who can transform data findings into recommendations to compose reports and executive level presentations
Strategic thinkers People who enjoy analyzing data or trends for the purposes of planning, forecasting, advising, budgeting, reporting, or sales opportunities
Collaborative partners People who build and leverage cross-functional relationships to bring together ideas, data and insights to drive continuous improvement in functions
Dedicated achievers People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations
Effective communicators People who can interpret information clearly and accurately to concisely communicate results and recommendations to stakeholders, senior management, and cross-functional teams

What you will do

As a Clinical Medical Affairs Program Manager, you will provide advanced scientific writing expertise to the regulatory, clinical and other functional area teams, ensuring successful preparation of high-quality submission-ready documents and marketing medical materials, which includes developing and maintaining Clinical Evaluation Reports (CERs), addressing Regulatory Body questions requiring clinical data support and collaborating on a number of other clinical and regulatory documents You will serve as the scientific writing content expert for the department You will be the clinical science liaison with internal customers and regulatory agencies regarding product safety and performance

Clinical Regulatory Management

Serves as medical writing lead on clinical regulatory documents such as those associated with filings and dossiers, including writing and maintaining CERs
Converts relevant data and information into a form that meets clinical regulatory document requirements Explains data in manner consistent with the target audience(s), journal/congress requirements, and/or clinical regulatory requirements Coordinates the review, approval, and other appropriate functions involved in the production of scientific publishing or clinical regulatory projects
Collaborate with RA on all phases of regulatory submissions and approvals, including clinical document preparation and review, the formulation of responses to regulatory agencies and other clinical regulatory documentation
Drive a culture of continuous improvement in the Medical Writing processes, incorporating new or updating regulatory requirements

Medical and Technical Writing

Coordinate the completion of clinical science documents including writing study reports
Converts relevant data and information into a form that meets clinical regulatory document requirements Explains data in manner consistent with the target audience(s), journal/congress requirements, and/or clinical regulatory requirements Coordinates the review, approval, and other appropriate functions involved in the production of scientific publishing or clinical regulatory projects
Collaborate with other teams on clinical study reports, clinical evidence gap assessments, marketing collaterals, PMCF reports, systematic literature searches, publications and other documents that require the evaluation of clinical data and/or clinical literature

Profile Summary:

Employment Type : Full Time
Eligibility : Any Graduate
Industry : Manufacturing/Industrial, Healthcare
Functional Area : Bio Tech/R&D/Scientist
Role : Clinical Research
Salary : As per Industry Standards
Deadline : 09th Jun 2020

Key Skills:

These are some of our most popular tutorials

People who search this job also searched for the following Keywords

Salary trends based on over 1 crore profiles

View Salaries

All rights reserved © 2018 Wisdom IT Services India Pvt. Ltd DMCA.com Protection Status