Worldwide Clinical Trials

Associate, Proposals & Client Services - US - Remote

Worldwide Clinical Trials$54K — $107K *
US-AnywhereRemote in Durham, NC
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 0-2 years of experience in Clinical or Laboratory Operations, CRO or Pharmaceuticals
  • Excellent organizational, analytical, and mathematical skills
  • Ability to create customized budgets and assemble multiple documents
  • Experience drafting bids and proposals in a CRO environment preferred
  • Strong negotiation and conflict resolution skills
  • Proficiency in MS-Office applications including Word and Excel
  • Bachelor's Degree required, preferably in Life Sciences or Business

Responsibilities

  • Manage all aspects of assigned RFPs and RFIs from receipt to final delivery
  • Collaborate with Account Directors and Operational teams to refine proposals
  • Review scientific documents to integrate study information into budgets
  • Establish priorities and deadlines for proposal information gathering and approvals
  • Facilitate information collection from various sources and subject matter experts
  • Maintain and update CRM database and internal tracking programs

Benefits

  • Comprehensive benefits package depending on location
  • Commitment to pay equity and transparency
  • Support for an inclusive and equitable workplace
Full Job Description
What the Associate, Proposals and Client Services does at Worldwide

The Associate, Proposals and Client Services is responsible for the coordination, preparation and management of all requested proposals, RFIs and associated client service functions. This includes pricing and budget analysis, prioritization of client requests and interactions with all levels of Worldwide personnel to ensure efficient and comprehensive proposal preparation. The Proposals and Client Services Associate communicates with both scientific and business personnel to secure project scope, timelines and client special needs. In addition, this position maintains all internal tracking processes and customizes proposal templates for each client and opportunity.

What you will do

  • Responsible for all aspects of assigned RFPs and RFIs. Manages the overall proposal process from receipt of RFP/RFI to final delivery.
  • Work with Account Directors and Operational teams (i.e. clinical, bioanalytical and support services) to refine proposal scope and integrate solutions into complete proposals.
  • Review protocols and other scientific documents to apply appropriate study information to budget tools.
  • Meet proposal deadlines by establishing priorities and target dates for information gathering, writing, reviews and approvals.
  • Act as facilitator for collection of information from various sources. Work with subject matter experts to gather information and customize content.
  • Maintain and update CRM database and internal tracking programs.


What you will bring to the role

  • Strong planning, strategizing, managing, monitoring, scheduling, and critiquing skills
  • Excellent written and verbal communication skills to clearly and concisely present information
  • Strong interpersonal skills in a fast-paced, deadline oriented, and changing environment
  • Excellent ability to handle multiple tasks and many details in a fast-paced and constantly changing environment
  • Ability to exercise sound judgment and make decisions independently
  • 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


Your experience

  • Prefer 0-2 years of experience in Clinical or Laboratory Operations, CRO/Pharmaceuticals
  • Ability to demonstrate excellent organizational, analytical and mathematical skills
  • Skilled in creating customized budgets and ability to assemble multiple documents/responses
  • Experience drafting bids and proposals in a CRO environment preferred
  • Ability to advise and interact with all levels of management including negotiation and conflict resolution skills
  • Proficiency in all MS-Office applications including Microsoft Word and Excel
  • Bachelor's Degree required (prefer degree in Life Sciences or Business)


At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation.

The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):

United States of America - $54,500.00 - $107,500.00

The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.

About Worldwide Clinical Trials

Worldwide Clinical Trials is a global contract research organization (CRO) that provides clinical research services to pharmaceutical and biotechnology companies. They specialize in early phase development, late phase development, and full-service clinical research. Worldwide Clinical Trials has experience in a wide range of therapeutic areas, including oncology, neuroscience, and infectious diseases. They are committed to providing high-quality, efficient, and cost-effective services to their clients.
Learn more about Worldwide Clinical Trials
Size
1,500 employees
Industry
Founded
1986

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