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Altasciences

Integrated CRO for early-phase drug development

Associate Director, Ligand Binding Assay

Biology & BiotechConfirmed live in the last 24 hours
Full-timeHarleysville, PA, USAIn-person

About the Job

Requirements

  • A Ph.D. in Chemistry, Biochemistry, Biology, or Pharmacology with at least five years of relevant experience.
  • An M.Sc. with at least seven years of relevant experience.
  • A B.Sc. with at least ten years of relevant experience in bioanalysis, or other pertinent laboratory-based qualifications in a CRO or pharmaceutical company in lieu of a Ph.D.
  • At least five years of related experience.
  • At least three years of related supervisory experience in a multidisciplinary environment.
  • Proficiency with Microsoft Word, Excel, Outlook, and PowerPoint.
  • Ability to read and interpret technical documents and industry-specific manuals.
  • Ability to write advanced reports and correspondence.
  • Ability to speak effectively before groups of customers or employees of the organization.
  • Well-developed interpersonal skills.
  • Personal and professional integrity and discretion in handling confidential information.
  • Ability to develop trusting relationships to gain support and achieve results.
  • Ability to manage multiple conflicting priorities.
  • Ability to work independently, stay motivated, take initiative, identify and anticipate client needs, and make implementation recommendations.

Responsibilities

  • Provide scientific and technical leadership in the area of expertise within the Laboratory Sciences department.
  • Manage direct reports, provide scientific support, and ensure their performance, productivity, and efficiency in project assignments.
  • Participate in professional internal and external presentations, scientific outreach, and conferences.
  • Manage assigned personnel, including scheduling projects, training and development, providing regular direction and performance feedback, taking disciplinary actions, and preparing and delivering annual performance and salary reviews.
  • Scientifically review driving documents and reports and raise pertinent issues to senior management.
  • Contribute to financial success through revenue and gross margin targets and client satisfaction.
  • Ensure scientific staff meet quality and regulatory requirements and promptly resolve quality and key performance indicator issues.
  • Ensure continued operational improvements for efficiency and cost control in areas of expertise.
  • Provide scientific support to assigned Bioanalytical Responsible Scientists, Contributing Scientists, or Principal Investigators; ensure project timelines are respected; communicate delays promptly to internal and external stakeholders; and recommend resource adjustments when needed based on deliverable schedules.
  • Serve as a Bioanalytical Responsible Scientist, Contributing Scientist, or Principal Investigator when assigned.
  • Set up and implement training for technical and scientific ligand binding assay staff.
  • Improve laboratory efficiency, including assay scheduling, operations, and workflows.
  • Review costing assessments and schedule projects with Business Development and Operations.
  • Contribute to the growth and development of ligand binding assay services and participate in strategic planning.
  • Work closely with other management members and serve as backup when other Laboratory Sciences leaders are out of office.
  • Respect health and safety standards for personal protection, laboratory maintenance, and work procedures.
  • Act as Test Site or Facility Management for applicable validation and sample analysis studies and method approval, as needed.
  • Perform other duties as assigned.

Desired Qualifications

  • Relevant industry experience.

About the Company

Altasciences

Integrated CRO for early-phase drug development

Altasciences provides integrated early-stage drug development services, covering preclinical testing, early clinical trials, and contract manufacturing. It functions as a single, in-house CRO that coordinates discovery support, safety testing, clinical research, and manufacturing to streamline a program from start to early proof of concept. The company differentiates itself by offering an end-to-end, one-stop path rather than requiring clients to contract multiple vendors. Its goal is to help innovator programs move quickly and efficiently through early development to speed up decision making and progression to later-stage trials.

Company size
1,001-5,000
Company stage
Early VC
Total funding
$6.7M
Headquarters
Laval, Canada
Founded
1976

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