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Senior Strategic Content Writer of Commercial Solutions

Employer
Worldwide Clinical Trials - USA
Location
Raleigh, North Carolina, United States
Salary
Competitive
Start date
7 Nov 2022
Closing date
6 Dec 2022

View more

Discipline
Marketing, Corporate Affairs
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details

Who we are

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,000 experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for other s who value this same pursuit

What you will do

Tasks may include but are not limited to:
  • Create customized deliverables for specific client requests (library, playbook, layout, design, etc.)
  • Independently drive and own assigned projects
  • Respond to routine and non-routine inquiries in a timely and professional manner
  • Resolve complex inquiries with minimal support or oversight
  • Interact with management to ensure alignment on projects across the department and organization
  • Support assigned initiatives for process improvement (text templates, case studies, biographies, playbooks)
  • Proofread, edit, rewrite, and revise materials to ensure readability and consistency of message and tone.
  • Be a champion for the company guidelines for writing based deliverables (style guides, etc.) and aid others with queries regarding the content and application of these rules as necessary
  • Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.
  • Excellent analytical skills, oral and written communications, strong attention to detail, prioritization, self-motivation, and time management proficiencies
  • Ability to handle multiple tasks and many details in a fast-paced and constantly changing environment, working either independently or in a team environment depending on the task
  • Ability to exercise sound judgment and make decisions independently
  • Comprehensive understanding of the commercial development process, and the overall business organization, functional areas, and commercial strategy

Your experience
  • Bachelor’s degree required; Master’s degree preferred.
  • Minimum of five to seven years of professional work experience as a writer and editor that required versatility, meeting deadlines, high standards, and careful attention to detail.
  • Exceptional communication, writing and editing skills, and experience working with a wide variety of constituents
  • Advanced fact-checking and proofreading skills
  • Positive, problem-solving attitude and ability to think strategically
  • Experience working collaboratively and constructively with business development, project managers, and communicators across an organization
  • Demonstrated project management, planning, and organizational skills
  • Experience with analyzing large data sets and characterizing information
  • Excellent customer relationship management skills and strong commercial acumen
  • Ability to work in a high pressure or time-sensitive environment including the ability to handle multiple issues on multiple projects simultaneously
  • Proven ability to build peer relationships and effective teams with demonstrated global and cultural awareness
  • Minimum five years’ experience in the CRO and/or pharmaceutical industry or similar preferred
  • Experience within a CRO or Pharma company providing comprehensive understanding of sponsor/CRO business practices and advanced knowledge of operational/financial practices, with the ability to analyze and evaluate processes and procedures preferred
  • Strong computer skills, including knowledge of Microsoft Office suite (Excel, PowerPoint, and Word), and Adobe Acrobat Professional.
  • Ability to work with minimal supervision

Why Worldwide

At Worldwide, we balance fun with the serious business of changing lives. We have a values-driven culture that is built from the ground up. We empower our team members to treat every clinical trial like a patient’s life depends on it - because it does.Our leaders are in the trenches with you - committed to advancing science and moving mountains for our customers.

Interested in hearing more about Worldwide or our roles? Check out our careers page at www.worldwide.com/careers!

Company

Find out more about working for our company

Worldwide Clinical Trials -hub-button

Brief Company Description; 

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 2,000 experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.

Company info
Mini-site
Worldwide Clinical Trials - USA
Location
600 Park Offices Drive
Suite 200
Research Triangle Park
NC 27709
United States

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