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Veeva Clinical Jobs in Raleigh, NC (NOW HIRING)

AskBio

Manager, Data Management

Durham, NC · On-site

Prior use of and/or familiarity with clinical trial database packages such as Veeva EDC, Medidata Rave * Significant knowledge of the drug development process, clinical trial methodology, data ...

NCSL International

Process Engineer

Morrisville, NC · On-site

$100 - $125/hr

The Process Engineer drives operational productivity in our automated and regulated clinical ... Experience in using enterprise level software systems including ServiceNow, Veeva, Git, Confluence ...

IQVIA

Regulatory Project Manager

Durham, NC · On-site

$97K - $270K/yr

... Veeva RIM would be beneficial. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We ...

IQVIA

Regulatory Project Manager

Durham, NC · On-site

$97K - $270K/yr

... Veeva RIM would be beneficial. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We ...

IQVIA, Inc.

Regulatory Project Manager

Durham, NC · On-site

$97K - $270K/yr

... Veeva RIM would be beneficial. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We ...

IQVIA LLC

Regulatory Project Manager

Durham, NC · On-site

$150 - $200/hr

... Veeva RIM would be beneficial. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We ...

IQVIA, Inc.

Senior Project Lead Field Director

Raleigh, NC · On-site

$200K - $240K/yr

Veeva / Sales Force.com Database experience. Note: This role is not eligible for visa sponsorship ... clinical research services, commercial insights and healthcare intelligence to the life sciences ...

IQVIA

Senior Project Lead Field Director

Raleigh, NC · On-site

$200K - $240K/yr

Veeva / Sales Force.com Database experience. Note: This role is not eligible for visa sponsorship ... clinical research services, commercial insights and healthcare intelligence to the life sciences ...

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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 the key skills and qualifications needed to thrive as a Veeva Clinical specialist?

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 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 popular job titles related to Veeva Clinical jobs in Raleigh, NC?

For Veeva Clinical jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Veeva Clinical jobs in Raleigh, NC look for?

The top searched job categories for Veeva Clinical jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Veeva Clinical jobs?

Cities near Raleigh, NC with the most Veeva Clinical job openings:

Veeva Clinical jobs near you
Infographic showing various Veeva Clinical job openings in Raleigh, NC as of September 2026, with employment types broken down into 100% Full Time. Highlights an 60% In-person, and 40% Remote job distribution.

Manager, Data Management

AskBio

Durham, NC • On-site

Full-time

Posted 19 days ago

Job description

Opportunity for Secondment to AskBio
We're pleased to share an exciting secondment opportunity at AskBio.
This role is available for a time period to be determined by leadership at both Bayer and AskBio. While most assignments range from one to two years, the exact duration will be based on business needs and mutual agreement.
This secondment offers a unique chance to broaden your experience, expand your knowledge, and contribute meaningfully to AskBio's mission: to advance gene therapy and change the lives of patients around the world.
If you're interested in exploring this opportunity, we encourage you to:
  • Speak with your direct manager to discuss your interest and alignment with your development goals.
  • Apply directly using the link provided in the posting.

We look forward to seeing how our colleagues continue to grow and make an impact across the Bayer-AskBio partnership.
Our vision: Pioneering science to create transformative molecular medicines.
Our mission: Lead innovative science and drive clinical outcomes to transform people's lives.
Our principles:
  • Advance innovative science by pushing boundaries.
  • Bring transformative therapeutics to patients in need.
  • Provide an environment for employees to reach their fullest potential.

Our values:
  • Be a Pioneer. We are not afraid of the impossible and to innovate to make gene therapies accessible to those in need.
  • Cultivate Collaboration. Strive to be the best teammate, actively listen, openly communicate, and embrace diverse points of view.
  • Embrace Responsibility. We are humbled by the enormity of our mission. We hold a relentless commitment to advance science and clinical outcomes for our patients, families, and caregivers.
  • Raise the Bar. Continuously drive improvements and efficiencies. Seek and provide constructive feedback. Have a bias for learning and action.
  • Act with Uncompromising Integrity. Be honest, transparent, and committed to doing what's right in every situation. Make clear commitments and follow through.

Position Summary
We have an opportunity for Manager, Clinical Data Management to join the AskBio team in our RTP, North Carolina, location and be part of our continued success!
The Manager, Clinical Data Management, provides oversight of all data management activities outsourced to external suppliers and/or conducted in-house, from study set-up, to conduct and close out. including but not limited to database design specification development, database design programming, database User Acceptance Testing (UAT), database deployment to research sites, data review and database lock and data archiving. Therefore, ensure the quality and integrity of all databases used in AskBio sponsored trials.
This position will report to the Senior Director, Data Management.
Job Responsibilities
  • Ensure that end-to-end Data Management activities are conducted in accordance with high ethical and quality standards, all applicable GCP regulations and company procedures
  • Provide oversight of all data management activities outsourced to external suppliers and/or conducted in-house, including but not limited to Data Management Plan, database specification development, database design programming, database User Acceptance Testing (UAT), database deployment to research sites, data review, coding and database locks
  • Efficiently plan, coordinate, and deliver complete, high quality and reliable clinical trial data in a timely manner for assigned projects
  • Serve as the DM point of contact for internal and external study team members with minimal oversight from senior data management resources
  • Provide strong quality and project oversight over third-party vendor responsible for data management deliverables
  • Take a leadership role to gather content and integration requirements for EDC and close collaboration with partners supporting other data collection systems (Non-EDC Data)
  • Represent DM on cross-functional project teams & submission teams
  • Provide support for Health Authority inspections and audits
  • Effectively manage changes to database design and data management requirements as necessary due to protocol amendments and changes to overall clinical development programs
  • Develop, troubleshoot, and maintain complex programs and utilities leading to database design, creation, validation, & use as well as clinical trial statistical analysis
  • Participate in the development of departmental standard operating procedures, working procedures and guidance documents

Minimum Requirements
  • Bachelor's degree in life sciences, statistics, biostatistics, mathematics, computer science, biotechnology or related field with a minimum of 6 years' clinical trial related data management experience
  • Prior use of and/or familiarity with clinical trial database packages such as Veeva EDC, Medidata Rave
  • Significant knowledge of the drug development process, clinical trial methodology, data management & statistics and relevant regulatory requirements for drug approval
  • Demonstrated ability to operate and lead in a matrix organization, building successful working relationships and effective stakeholder management in an environment that requires diverse educational and functional expertise

Preferred Education, Experience and Skills
  • Good knowledge of CDASH® standards and how they support CDISC® standards (SDTM). Hands on experience of confirming database design and DM principles are consistent with all types CDASH® of and their support of SDTM
  • Experience managing multiple sources of data
  • Experience identifying and mitigating potential risks in the DM space; problem resolution skills to solve errors/inconsistencies found in data processing to reduce risk to data integrity and validity
  • Experience in managing gene therapy studies
  • Excellent verbal and written communications skills; able to communicate proactively and effectively
  • Utilizing and developing SAS, SQL, Power BI, Excel and other analytical tools to support clinical data review, identifying data trends and discrepancies, and monitoring study performance metrics

AskBio Inc. (AskBio) is an Equal Opportunity Employer and does not discriminate against any employee or applicant for employment because of race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status or any other protected status prohibited under Federal, State or local laws. All employment decisions are based on valid job-related requirements. If you are a qualified individual with a disability or a disabled veteran and are unable or limited in your ability to use or access our website, you may request a reasonable accommodation to express interest in a specific opening by calling us at (919) 561-6210 or sending us an email at talent@askbio.com.

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