Biometrics and PV Business Support Manager

Posted 8 Days Ago
Be an Early Applicant
Hiring Remotely in England, GBR
Remote
Senior level
Biotech • Pharmaceutical
The Role
Oversee and coordinate business development activities for Biometrics and Pharmacovigilance, including bids, proposals, RFIs, budgets, change orders, statements of work, and presentations. Develop and edit proposal materials, coordinate subject matter experts and vendors, track deadlines, identify proposal trends, maintain RFI resources and bid-defense materials, and provide training to colleagues.
Summary Generated by Built In

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 Biometrics and PV Business Support Manager does at Worldwide

You will be responsible for the oversight and co-ordination of all Business Development activities within the Biometrics and Pharmacovigilance department, including but not limited to bids and proposals, response to RFI’s and monitoring and co-ordination of change orders.
What you will do
 

  • Have oversight of and maintain and track all active bids and proposals across the department

  • Have oversight of and co-ordinate, monitor and track all change orders within the department

  • Triage proposals /budgets based on requirement for SME input. In first instance develop triage criteria with the SMEs.

  • For proposal/budgets not requiring SME input develop budgets according to agreed standards and similarly develop proposal text based on standards.

  • For proposals/budgets requiring SME input develop draft budgets and proposal text for review.

  • Respond to RFPs and RFIs, develop bids and proposals, statements of work, presentations, and other materials that support the Biometrics and PV input into Business Development activities

  • Work with Account Directors, operational teams and 3rd party vendors to integrate solutions into complete proposals and statements of work.

  • Identify trends in proposals that may require a change in departmental strategy.

  • Proofread, edit, rewrite, and revise documents to ensure readability and consistency of message and tone.

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

  • Work with subject matter experts to gather information and customize content.

  • Respond to routine and non-routine enquiries in a timely and professional manner. Obtain assistance to resolve complex enquiries, in order to discuss and learn.

  • Provide budget tool and proposal training and mentoring for Biometrics & PV colleagues as required.

  • Maintain standard proposal and bid defense slides for Biometrics and PV.

  • Maintain departmental RFI Library

  • Other duties as requested or assigned by supervisor.

  • 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 bring to the role
 

  • Sound understanding of Biometrics and PV operations.

  • Strong planning, managing, monitoring, scheduling, and critiquing skills

  • Excellent written and verbal communication skills to clearly and concisely present information

  • Strong interpersonal skills to work in a dynamic team with a variety of personnel in a fast-paced, deadline oriented environment

  • Excellent ability to handle multiple short-term assignments and project deliverables with strict deadlines in a constantly changing environment

  • Ability to exercise sound judgment and make decisions independently

  • Excellent self-motivation skills

  • Proficiency in all MS-Office applications including Microsoft Word and a high level of Excel

  • Ability to train other personnel

Your experience
 

  • Minimum 5 years’ experience in CRO operations involving one of Data Management, Biostatistics or PV

  • Bachelor's Degree required (prefer degree in Life Sciences, Communications, Journalism or Marketing).

  • Experience drafting bids and proposals in a CRO environment, or in pharma/biotech outsourcing preferred

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

  • Ability to advise and interact with all levels of management

  • Ability to demonstrate excellent analytical and mathematical 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.

Skills Required

  • Minimum 5 years of CRO operations experience involving Data Management, Biostatistics, or Pharmacovigilance
  • Bachelor’s degree
  • Sound understanding of Biometrics and Pharmacovigilance operations
  • Strong planning, management, monitoring, scheduling, and critiquing skills
  • Excellent written and verbal communication skills
  • Strong interpersonal skills in a fast-paced, deadline-oriented environment
  • Ability to manage multiple short-term assignments and project deliverables under strict deadlines
  • Ability to exercise sound judgment and make independent decisions
  • Self-motivation
  • Proficiency in Microsoft Office applications, including advanced Excel skills
  • Ability to train other personnel
  • Experience drafting bids and proposals in a CRO, pharma, or biotech outsourcing environment
  • Knowledge of the CRO and pharmaceutical industries and sales support activities
  • Understanding of study design, project management, and operational requirements for study implementation
  • Ability to advise and interact with all levels of management
  • Excellent analytical and mathematical skills
  • Degree in Life Sciences, Communications, Journalism, or Marketing
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The Company
HQ: Research Triangle Park, NC
2,566 Employees

What We Do

About Worldwide Clinical Trials  Worldwide Clinical Trials is a global, midsize contract research organization (CRO) that provides top-performing bioanalytical and Phase I-IV clinical development services to the biotechnology and pharmaceutical industries.   Founded in 1986 by physicians committed to advancing medical science, our full-service clinical experience ranges from early phase and bioanalytical sciences through late phase studies, post approval, and real-world evidence. Major therapeutic areas of focus include cardiovascular, metabolic, neuroscience, oncology, and rare diseases. Operating in 60+ countries with offices in North and South America, Eastern and Western Europe, and Asia, Worldwide is powered by its more than 3,000 employee experts.   For more information, please visit www.worldwide.com or connect with us on Twitter, LinkedIn, Facebook, and Instagram.

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