Director, Clinical Data Management at Definium Therapeutics

United States

$208.4k - $234.737k

Definium Therapeutics, formerly known as Mind Medicine, is a clinical stage biopharmaceutical company developing novel product candidates to treat brain health disorders. Our mission is to be the global leader in the development and delivery of treatments that unlock new opportunities to improve patient outcomes. We are developing a pipeline of innovative product candidates, with and without acute perceptual effects, targeting neurotransmitter pathways that play key roles in brain health. Founded in 2019, we are continuously expanding our presence and global footprint. We are constantly searching for high-impact individuals in various clinical, technical and business operations domains to strengthen our team of patient-centric, intelligent individuals. Responsibilities: Oversee CDM operations including CRF/eCRF design, validation programming, discrepancy management, and database development/production Provide oversight of CROs, vendors, and internal teams to maintain quality standards and performance metrics Ensure CDM documentation, SOPs, and processes support high data quality, integrity, and regulatory compliance with FDA, GCP, ICH, and GCDMP requirements Partner within Biometrics and Data Science as well as cross-functionally on data management issues and alignment Recruit, develop, motivate, and provide leadership to CDM staff and consultants Support resource planning, budget forecasting, timelines, and issue resolution for ongoing clinical trials Identify risks and challenges in clinical trial data management and propose solutions to maintain timelines and quality Escalate strategic, budgetary, or cross-functional issues when broader leadership input is required Ability to meet deadlines, prioritize workload, and handle multiple priorities simultaneously Experience with data visualization tools (e.g., Elluminate) (preferred) Must maintain an inspection-ready environment and support regulatory readiness Willingness to travel as needed Qualifications: Bachelor’s or Master’s degree in a scientific subject area Minimum of 8 years CDM experience in a pharmaceutical, biotech or CRO setting At least 4 years of line management experience Global or international experience is required Strong experience in cross functional leadership, clinical trial execution, vendor oversight, and inspection readiness Sophisticated knowledge of CDM processes, EDC systems, database programming, quality management and technology trends In-depth knowledge of FDA regulations, GCP, GCDMP, CDASH/CDISC, and ICH guidelines Strong leadership, mentoring, recruiting and team development skills Excellent communication, interpersonal, influencing and negotiation skills Strong problem-solving, analytical thinking, prioritization and organizational skills Ability to manage multiple priorities, adapt to changing business needs, and work collaboratively across functions The starting base pay range for this position is $208,400.00 - $234,737.00. Compensation will be determined based on several factors including, but not limited to, skill set, years of experience, and the employee’s geographic location. Employees in this role may be entitled to additional compensation, including bonus and equity. Benefits information is listed on our Jobs Page. The Company provides competitive benefits to employees including: 100% paid health benefits including Medical, Dental and Vision for you and your dependents 401(k) program with company match and vesting after the turn of the first month after your start date Flexible time off Generous parental leave and some fun fringe perks!