Irt Project Manager Jobs in Ohio (NOW HIRING)

Are you interested in shaping clinical studies from A to Z while overcoming both technical and organizational challenges? Then join our team and help us shape the future of pain therapy!

At Vertanical, you can look forward not only to exciting clinical study projects, but also to the opportunity to apply your expertise in data management and analysis at the highest level. You will actively help shape the future of innovative cannabinoid-based medicinal products and work closely with a highly motivated team. You are not only detail-oriented but also strategic, transforming data into groundbreaking insights. If you are eager to help build processes from the ground up and take on responsibility, you have come to the right place!

• You will be responsible for Clinical Data Management for clinical studies from conception through database closure, ensuring high data quality and the timely achievement of milestones.
• You will develop and review Data Management Plans, Data Validation Plans, edit check specifications and other study-specific documentation.
• You will lead the selection, management and technical collaboration with CROs and other service providers in the area of Clinical Data Management.
• You will be responsible for the design, set-up and quality assurance of eCRF, IRT, eCOA and ePRO systems, including questionnaire implementation, licensing matters and validation.
• You will manage the programming, execution and documentation of user acceptance testing, as well as the release of databases and system changes.
• You will plan and coordinate ongoing data reviews, data cleaning, query management, external data reconciliations and the follow-up of data quality risks.
• You will ensure the reconciliation of the clinical database with safety and laboratory databases.
• You will prepare data review meetings, present data quality metrics and jointly derive appropriate actions with the relevant functions.
• You will be responsible for preparing and conducting database locks, including freeze, lock and archiving activities, as well as the required documentation.
• You will further develop processes, work instructions and standards in Clinical Data Management and support audits, inspections and responses to data management-related questions.

• You have completed a Master’s degree or PhD in natural sciences, medicine, pharmacy, biostatistics, data science or a comparable field.
• You have several years of professional experience in Clinical Data Management, ideally in the pharmaceutical industry, at a biotech company or at a CRO.
• You have extensive experience in the planning, execution and documentation of clinical studies, as well as across the entire data management lifecycle.
• You have practical experience with common eCRF and EDC systems such as Medidata Rave, Oracle Clinical, Veeva EDC, Castor EDC or comparable platforms.
• You are confident in working with Data Validation Plans, edit checks, query management, data reviews, external data reconciliations and freeze and lock processes.
• You have experience managing CROs and service providers and communicate with internal and external stakeholders in a confident, professional and reliable manner.
• You are familiar with relevant GCP requirements and regulatory expectations regarding data integrity, computerized systems and clinical data processes.
• You work independently, in a structured, analytical and solution-oriented manner, have a strong quality mindset and maintain an overview even when managing several studies in parallel.
• Experience with SAS, R, Python or SQL, as well as knowledge of data analysis and visualization, is desirable.
• You have business-fluent German and English language skills (at least C1 level).

Vertanical is a globally leading biopharmaceutical company specializing in the development and commercialization of innovative medicinal products for the treatment of chronic pain. We pursue a clear vision: a world free from chronic pain! With VER-01, we have developed a unique cannabinoid-based medicinal product for the treatment of chronic pain, which was approved in Germany and Austria in June 2026 under the name Exilby. Following more than eight years of intensive research and development, this marks a significant milestone for us. Approval in the United States is planned for 2029. Our goal is to establish Exilby as the leading treatment for chronic pain by 2030, thereby setting new standards in pain therapy. Does this sound exciting to you?

We offer you a diverse and challenging position with exciting responsibilities and extensive opportunities to make a difference. Our innovative environment enables you to realize your professional potential through short decision-making processes, responsibility from day one and the freedom to pursue new approaches. You can look forward to personalized learning opportunities and meaningful work. Through your individual contribution, you will help give millions of people a new lease on life!

We look forward to getting to know you.
Please feel free to contact your designated representative directly:
FUTRUE GmbH
Vanessa Köpfler
Am Haag 14
82166 Gräfelfing
jobs@futrue.com
https://futrue.com
For ease of readability, the masculine form is used in this job advertisement. It expressly refers to all genders (m/f/d).