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Senior Proposal Manager - Writing - LATAM - Remote

Role overview

Qualifications

  • Five+ years of experience in CRO/pharma BD or proposal management in a relevant environment
  • Excellent writing, editing, proofreading, and proposal development skills with ability to deliver high-quality proposals on time; proficiency in Word, PowerPoint, Excel
  • Proven leadership and mentoring abilities in a matrixed environment; ability to influence executive and C-suite contributors
  • Bachelor’s degree required; master’s or PhD preferred; knowledge of CRO/pharma industry, study design, project management; strong verbal/written communication; strong customer relationship and commercial acumen

Responsibilities

  • Lead writing, coordination, and presentation of responses in Word, PowerPoint, and other formats; manage the proposal development process with Account Directors and SMEs
  • Gather and customize content with SMEs; collate proposal content from internal sources; ensure offerings are clearly articulated and meet deadlines with defined priorities
  • Proofread, edit, rewrite, and revise documents for readability, accuracy, and consistency; respond to routine and non-routine inquiries in a timely and professional manner
  • Own and drive proposal writing resource and process improvement initiatives; provide mentorship to junior writers, onboarding and ongoing development

Key facts

Other skills

  • Microsoft PowerPoint
  • Microsoft Word
  • Analytical Skills
  • Strategic Thinking
  • Business Acumen
  • Microsoft Excel
  • Negotiation
  • Editing
  • Decision Making
  • Non-Verbal Communication
  • Multitasking
  • Time Management
  • Detail Oriented
  • Team Building
  • Prioritization
  • Social Skills
  • Self-Motivation
  • Problem Solving

About the company

Worldwide Clinical Trials logo

Worldwide Clinical Trials

Contract Research Organizations (CRO)

About Worldwide Clinical Trials  Worldwide Clinical Trials is a leading full-service global contract research organization (CRO) that works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new treatments. Our capabilities include bioanalytical laboratory services, Phase I-IV clinical trials, and post-approval and real-world evidence studies – all powered by our team members who bring their expertise and a collaborative, personalized approach to each clinical program. Anchored in our company’s scientific heritage, our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, is applied to develop flexible plans and solve problems quickly for our customers. Our talented team of 3,000+ professionals spans 60+ countries, and embraces a culture of diversity, equity, inclusion, and belonging (DEI&B). We are united in cause with our customers to improve the lives of patients through new, innovative therapies. For more information on Worldwide, visit www.Worldwide.com.

Company details

Company typeLarge
IndustryContract Research Organizations (CRO)
Company size1001 - 5000

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Job description

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 3,500+ 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 others who value this same pursuit.

Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!

What the Senior Proposal Manager - Writing does at Worldwide Clinical Trials

The Senior Proposal Manager – Writing leads proposal writing responsibilities for assigned projects, supports proposal writing resource and process improvement initiatives, and mentors junior proposal writers. This role works with Account Directors, subject matter experts (SMEs), and other Worldwide Clinical Trials personnel.

Your responsibilities

  • Develop robust proposals, leading the writing, coordination, and presentation of responses in Word, PowerPoint, and other systems or formats

  • Work with Account Directors and SMEs to effectively manage the proposal development process

  • Actively participate in project strategy discussions, ensuring product and service offerings are clearly articulated in proposals

  • Proofread, edit, rewrite, and revise documents to ensure readability, consistency, accuracy, and relevance

  • Meet proposal deadlines by establishing priorities and target dates for information gathering, writing, reviews, approvals, and signatures

  • Act as a focal point to collect information from various sources

  • Collaborate with SMEs to gather information and customize content

  • Collate proposal content independently as much as possible from team discussions and internal sources such as libraries, requesting direct content from SMEs only when primary sources are not available

  • Respond to routine and non-routine inquiries in a timely and professional manner

  • Apply strategic and customized solutions to proposal development

  • Take increased responsibility for owning, driving, and supporting proposal writing resource and process improvement initiatives, collaborating with junior proposal writers, proposal writing managers, and SMEs

  • Provide a high level of mentorship to junior proposal writers, including onboarding, training, and ongoing learning and development

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.

What you will bring to the role

  • Robust writing, project management, and time management skills to complete proposals on time and with high quality

  • Ability to mentor junior proposal writers in writing, project management, and industry knowledge to complete proposals on time and with high quality, and to keep the content library updated and accurate

  • Proven leadership skills in a matrixed environment and proven ability to effectively influence executive and C-suite team members regarding their contributions to client deliverables

  • Comprehensive understanding of the proposal development process, the overall business organization, functional areas, and commercial strategy

  • Excellent analytical, oral, and written communication skills; strong attention to detail; and prioritization and time management skills

  • Strong interpersonal skills and ability to effectively multitask in a fast-paced, deadline-oriented, and dynamic environment

  • Ability to exercise sound judgment and make decisions independently

  • Excellent self-motivation

  • Proficiency in all Microsoft Office applications, especially Word, PowerPoint, and Excel

Your experience

  • Excellent customer relationship management skills and strong commercial acumen

  • Strong organizational agility, negotiation skills, and demonstrated drive for results

  • Proven ability to build peer relationships and effective teams with demonstrated global and cultural awareness

  • Minimum five years of experience in the Contract Research Organization (CRO) or pharmaceutical business development or operational environment, or as a Proposal Manager – Writing

  • Bachelor’s degree: master’s or PhD preferred (preferred fields include Life Sciences, Communications, Journalism, or Marketing)

  • Knowledge of the CRO and pharmaceutical industry, knowledge of sales support activities, and a strong understanding of study design, project management, and operational requirements for successful study implementation

  • Ability to analyze and evaluate processes and resources

  • Ability to work effectively with minimal supervision

  • Candidates must reside in Latin America and have outstanding verbal and written communication skills

Promotion to the next level is not automatic based on years of experience. Personnel are evaluated on proven competency, level of responsibility, and ability to work independently.

We love knowing that someone is going to have a better life because of the work we do. 

To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.

Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.

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Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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