Associate Director, Clinical Applications

We’re looking for purpose-driven, passionate individuals to join our team. From clinical to commercial to supporting functions, Lexitans believe in the common mission: to be the best ophthalmic product development organization to partner with. 

Overview

The Associate Director, Clinical Applications, will oversee the management and development of clinical applications within our research and development (R&D) environment. This role involves collaborating with an IT managed services provider to ensure the successful implementation and maintenance of clinical systems, and working with cross-functional teams to support clinical research and development activities.

Responsibilities

• Clinical Application Management:
• • Oversee the implementation, maintenance, and optimization of clinical applications.
  • Ensure the integrity, security, and compliance of clinical data within the applications.
  • Collaborate with the IT managed services provider and related vendors to integrate clinical applications with other systems.
• Project Management:
• • Lead projects related to the development and enhancement of clinical applications.
  • Manage project timelines, budgets, and resources to ensure successful project delivery.
  • Coordinate with stakeholders to gather requirements and provide regular project updates.
• Collaboration and Communication:
• • Work closely with clinical research teams to understand their needs and provide application support.
  • Facilitate communication between clinical teams, the IT managed services provider, and other stakeholders.
  • Represent the Clinical Applications function in cross-functional meetings and initiatives.
• Continuous Improvement:
• • Stay updated on industry trends and advancements in clinical applications.
  • Identify opportunities for process improvements and implement best practices.
  • Provide training and support to end-users to maximize the effectiveness of clinical applications.

Requirements

Education:

Required: Bachelor’s degree in related field (Life Sciences, Information Technology, Clinical Research); Advanced degree preferred

Experience:

Min 7 years’ experience in clinical applications management or related role; experience in CRO preferred

Skills:

• Familiarity with Salesforce CRM, electronic data capture (EDC) systems and clinical trial management systems (CTMS).
• Strong project management and organizational abilities.
• In-depth knowledge of clinical research processes and regulatory requirements.
• Proficiency in clinical applications and related technologies.
• Strong communication and interpersonal skills.
• Strong problem-solving skills
• Ability to present ideas in business-friendly and user-friendly language
• Exceptionally self-motivated and directed
• Keen attention to detail
• Ability to motivate in a team-oriented, collaborative environment
• Ability to travel as required by role. Limited overnight travel may be required.

Physical Requirements

Position requires: ordinary ambulatory skills and physical coordination sufficient to move about conference or meeting locations as required; ability to stand, walk, stoop, kneel, crouch periodically for prolonged periods of time; manipulation (lift, carry, move) of light to medium weights of 10-35 pounds; arm, hand and finger dexterity, including ability to grasp and type for prolonged periods of time; visual acuity to use a keyboard, computer monitor, operate equipment, and read materials for prolonged periods of time; ability to sit, reach with hands and arms, talk, and hear for prolonged periods of time.

Disclaimer:

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. Lexitas Pharma Services, Inc., at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. Lexitas Pharma Services, Inc., at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees.