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Veeva Clinical Jobs in Indiana (NOW HIRING)

Edwards Lifesciences Corporation

Maintain regular contact and collaborate with partner TMTT clinical teams, cross BU partners ... processes (e.g., Trifecta, Veeva Vault, Litmos) for both internal and external training.

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Veeva Clinical information

What is a Veeva Clinical professional?

A Veeva Clinical professional is someone who specializes in using the Veeva Vault Clinical Suite, a cloud-based platform designed to manage clinical trial processes and data in the life sciences industry. Their responsibilities often include implementing, configuring, and supporting Veeva Vault Clinical applications such as eTMF, CTMS, and Study Startup. These professionals help organizations streamline clinical operations, ensure regulatory compliance, and improve collaboration across trial teams. Their expertise is highly valued by pharmaceutical, biotech, and contract research organizations.

What are some common challenges faced by professionals working in Veeva Clinical roles, and how can they be addressed?

Professionals in Veeva Clinical roles often encounter challenges such as adapting to frequent software updates, ensuring data integrity across multiple studies, and coordinating with cross-functional teams like clinical operations and IT. Staying current with new features and best practices is essential to maximize the platform's capabilities. Proactive communication and ongoing training can help address these challenges, as well as building strong relationships with stakeholders to streamline workflows and resolve issues efficiently.

What are the key skills and qualifications needed to thrive as a Veeva Clinical Specialist, and why are they important?

To thrive as a Veeva Clinical Specialist, you need a solid understanding of clinical trial processes, data management, and life sciences regulations, often supported by a degree in life sciences or related fields. Familiarity with Veeva Vault Clinical Suite, electronic data capture (EDC) systems, and relevant certifications like Veeva Vault Administrator are highly valued. Strong analytical thinking, attention to detail, and effective communication are essential soft skills for collaborating with cross-functional teams and clients. These competencies ensure the optimization of clinical workflows, regulatory compliance, and successful implementation of Veeva solutions in clinical research environments.
What are popular job titles related to Veeva Clinical jobs in Indiana? For Veeva Clinical jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Veeva Clinical jobs in Indiana look for? The top searched job categories for Veeva Clinical jobs in Indiana are:
Veeva Clinical jobs near you

Clinical Development Trial Lead Assoc Dir

Globalchannelmanagement

Indianapolis, IN

Full-time

Posted 3 days ago

Job description

Clinical Development Trial Lead Assoc Dir requires:

  • Stamford, CT or Indianapolis, IN
  • 5+ years clinical research experience or relevant experience in a scientific or health-related field
  • Experience with oncology (early & late phase clinical trials)
  • Applied knowledge of project management methodology, processes and tools
  • Demonstrated ability to lead and work effectively cross-culturally with global colleagues and with TPOs
  • Be recognized as a leader with demonstrated ability to coach others in process expertise.
  • Embrace strategic organizational changes and lead others effectively through these, exhibiting flexibility to adjust quickly and effectively to frequent change and altered priorities
  • Ability to influence without authority
  • Previous experience working in cross-functional teams/ projects and/or ability to establish and maintain relationships Effective and influential communication, self-management, and organizational skills
  • Demonstrated ability to handle complex situations through problem-solving, critical thinking and navigating ambiguity Other Information/Additional
  • Minimum of 5 years clinical trial experience with a strong working knowledge of the clinical research process
  • Prior clinical trial site-level or affiliate experience
  • Prior experience with local/country regional requirements
  • Strong analytical skills Proficiency in use of project management tools and techniques (e.g., Critical Chain, Veeva, MS Project, MS Excel, MS PowerPoint, PowerBI)
  • Need to travel periodically to scientific/regional meetings
  • Associate Director, Clinical Development Trial Lead (CDTL)
  • Clinical Trial Process Leadership and Expertise
  • Leverage and demonstrate broad understanding of therapeutic, clinical drug development, and process expertise in order to influence study design and program-level decisions considering regional needs.
  • Recognize inter-relatedness of cross-functional activities and understand the impact of project decisions on the overall clinical trial. Look for opportunities to expand and deepen clinical trial process expertise across functional teams, regions, and external partners and make decisions on process and issues affecting study implementation and execution.
  • Be knowledgeable on the global and regional operating model; coordinate and facilitate obtaining regional input to provide to the study teams.
  • Project Management, and Regional Operational Knowledge

DUTIES:

  • Broader responsibilities at Therapeutic Area/ Molecule/Indication level (e.g. attending relative critical chain network builds, providing input on strategy).
  • Use project management skills, processes, and tools to develop and execute local, regional, and/or global clinical trials (CT) as described:
  • Scope - Understand the scope of work required to complete the clinical trial successfully. Monitor the status and make adjustments and changes (per change control process) as needed to meet the deliverables of the trial.
  • Timeline – Develop and track global trial enrollment plan by gaining alignment and integrating inputs across functions and geographies.