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Theradex Oncology

Full-service oncology CRO with regulatory support

Business Development - Clinical Services

Account ExecutiveUpdated on Nov 10
Full-timePrinceton, NJ, USA

About the Job

Requirements

  • A bachelor's degree in a life science field or equivalent is required.
  • At least 8 years of relevant business development experience in a CRO or pharmaceutical environment is required.
  • Experience with oncology clinical trials and cancer therapies is required.
  • High proficiency in core performance and leadership competencies is required.
  • Completion of the Theradex Oncology induction training program and ICH-GCP training is required.
  • Ability to anticipate project-related problems and develop and implement solutions is required.
  • Fluent written and verbal English is required.
  • Knowledge of the initiation, conduct, and completion of all phases of oncology clinical trials, study endpoints, and clinical databases is required.
  • Knowledge of identifying, anticipating, and reporting study-conduct problems to appropriate management, and developing solutions, is required.
  • Ability to write reports and varied correspondence is required.
  • Knowledge of the drug development process and the Theradex Oncology organizational structure is required.
  • Knowledge of current projects, including protocol and CRF details, study plans, project-specific scientific information, sponsor requirements, and applicable Theradex Oncology and sponsor SOPs, is required.
  • Thorough knowledge of current European and North American regulations and applicable guidelines, depending on location, is required.
  • Ability to set and meet personal short- and long-term goals is required.
  • Proficiency in the Microsoft Office Suite is required.
  • Ability to travel domestically and/or globally up to 50% when required is required.
  • A valid driver's license is required.

Responsibilities

  • Recruit new clients and support repeat business opportunities for Theradex.
  • Develop emerging business and the prospect pipeline.
  • Lead the contract process.
  • Facilitate client communications regarding the contract process and advise on change orders and quarterly reviews.
  • Prepare client proposals with support from area experts.
  • Prepare proposals and budgets, including scenario analyses and cost comparisons for internal and external use as needed.
  • Prepare Confidentiality Disclosure Agreements for prospective clients.
  • After project award, prepare the Master Service Agreement, initial Work Order Letter of Intent, or Consulting Agreement, following the appropriate review process.
  • Review contract performance quarterly and prepare supporting materials for client contract review meetings.
  • Maintain paper and electronic files of proposals, executed Master Service Agreements, Work Orders, Consulting Agreements, Letters of Intent, and supporting documentation.
  • Maintain a current list of Theradex experience organized by study phase and indication.
  • Work with clinical experts to prepare proposal-specific background information.
  • Coordinate bid defense meetings, prepare presentations, and participate in meetings as needed.
  • Update and maintain templates for client proposals, Master Service Agreements, Letters of Intent, and Consulting Agreements.

Desired Qualifications

  • A master's degree is preferred.
  • Basic knowledge of one or more European languages is an advantage, as applicable.

About the Company

Theradex Oncology

Full-service oncology CRO with regulatory support

Theradex Oncology provides full-service contract research organization support for cancer trials across all indications and modalities, backed by MD oncologists, regulatory experts, and experienced operations teams. It runs trials from start-up to close-out by combining medical oversight, regulatory submissions, clinical monitoring, data management, and site operations. Its distinct advantage comes from deep oncology specialization, decades of hands-on experience with biotech and pharma sponsors, and a track record with NCI-supported studies. Its goal is to help sponsors conduct efficient, compliant trials and generate reliable data to advance new cancer therapies to patients.

Company size
51-200
Company stage
Not listed
Total funding
Not listed
Headquarters
Princeton, NJ
Founded
1982

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