Strategic CRO Proposal Writer

Posted 8 Days Ago
Be an Early Applicant
Hiring Remotely in United States
Remote
Junior
Pharmaceutical
The Role
This role involves creating and refining client proposals and contracts, collaborating with project teams, conducting research, and ensuring alignment with client requirements while maintaining high quality and timely deliverables.
Summary Generated by Built In

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Home Based, US

Parexel's Strategic CRO Proposal Writer will bring several years of experience writing proposals within clinical (specifically Phase II, II & IV) will support the development of compelling, client-ready professionally presented proposals which exemplify the understanding of client requested requirements as transcribed from Client Relationship/Sales Directors, (CRD/CSDs), and the operational considerations as extracted from Functional Subject Matter Experts (SMEs).  Daily deliverables will be transcribed into highly tailored, differentiating proposal and contracting language for strategically identified opportunities and studies. They will help identify the most suitable output format for each proposal and will develop accordingly in Word, PowerPoint, online tools, or any other format that may become available in the future. This role will make recommendations to the Marketing and Proposals and Contracts Directors team as to how to incorporate best practices to all proposals.

Accountabilities:

  • Work alongside the assigned proposal and contract manager/specialist to produce compelling and differentiating text or slides for client proposals
  • Work closely with Integrated Solution Strategists (ISS), Client Relationship Directors (CRD) or Consultative Sales Directors (CSD) to perform appropriate client/indication/therapeutic area research to support proposal development

Add value to strategy meetings:

  • Identify issues and client requirements
  • Recommend proposal and study conduct strategy, and internal resourcing, based on experience
  • Support senior management and multi-disciplinary discussions to assure full and high-quality input
  • Establish agreement on timelines and deliverables from the strategy meeting, and follow-up to ensure adherence
  • Manage internal framework calls to ensure alignment with ISS and feasibility on content, structure and overall strategy

Write and create client specific proposal and contract text to:

  • Accurately reflect strategy discussions with compelling and differentiating content
  • Meet Parexel and client needs/expectation
  • Assure accuracy and appropriateness of text and attachments

Skills:

  • Strong understanding of the different operational aspects of clinical study conduct in different regions across the world, which may be demonstrated by previous work experience in the industry
  • Strong analytical and organizational skills with ability to perform several tasks simultaneously.
  • Consistently performs high quality work and delivers on time under pressure
  • Impressive writing skills to create compelling proposals
  • Excellent attention to detail, excellent oral/written communication skills along with highly developed interpersonal and strong team orientated skills.
  • Ability to work independently and without close supervision in order to meet deadlines.
  • Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail

Education:

  • Bachelor’s Degree in English, Life Science, Business, Languages or equivalent combination of education and experience.

EEO Disclaimer
Parexel is an equal opportunity employer.  Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

Top Skills

Online Tools
PowerPoint
Word
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The Company
HQ: Durham, North Carolina
20,524 Employees
On-site Workplace

What We Do

Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com.

Community Guidelines
Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are:

• Abusive, harassing or threatening to others.
• Defamatory, offensive, obscene, vulgar or depicting violence.
• Hateful targeting by race/ethnicity, age, color, creed, religion, gender,
sexual preference or orientation, nationality or political beliefs.
• Sexually explicit or pornographic.
• Fraudulent, deceptive, libelous, misleading or unlawful.
• Referencing criminal or illegal activity.
• Spamming.

We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.

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