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SDC is a team of diverse professionals providing exceptional Biometric Services, Consulting, and Technology Solutions to pharmaceutical, biologic, and medical device/diagnostic companies. Since 2005, our goal has been to partner with sponsors to supply high-quality and experienced team members to develop excellent medicines that save lives and cure diseases in the most efficient way possible. Our global team operates as a value partner to our clients, treating their needs as our own and delivering remarkable results. We are a specialty CRO providing scalable service offerings, focused services area specialists, efficient project timelines, optimal technology solutions, and proven success and experience. Our commitment to our clients is echoed in our commitment to our employees.
SDC's dedication to employee development is evident. We recognize achievements, provide growth opportunities and career advancement, offer a flexible work schedule, engaging work culture and employee benefits. We cherish our company culture and have a recognition program that promotes our core values of Energy, Integrity, Engagement, Innovation, Ownership, and Commitment. We aim to provide a sense of belonging for our employees with enjoyable activities orchestrated by SDC’s culture club. We are continually growing and innovating to support our clients and employees' needs, offering diverse perspectives that drive our growth in this constantly evolving industry.
The Clinical Data Manager is involved in all data management activities supporting clinical and/or non-clinical research studies for study initiation, setup, maintenance, and closeout. The role oversees daily data management project activities including timelines, budgets, staff, project scope, reports, and communication for the project's lifespan and mentors Clinical Data Analysts.
Candidates must reside in Arizona or along the U.S. east coast line. Unsolicited referrals from recruiting agencies for this or any open role will not be accepted unless a partnership has been established.
Primary responsibilities include performing study setup activities, allocating and prioritizing workloads for multiple projects, serving as a primary or backup resource for issues pertaining to data management, mentoring all levels of Clinical Data Analysts, maintaining quality control of data, and facilitating the review of medical coding for validity and completeness.
Candidates should be located in Arizona, Massachusetts, or North Carolina and have thorough knowledge of clinical trials and the role of clinical data management in the clinical trials process, excellent organizational and project management skills, and highly effective communication skills.
Benefits include opportunities for career advancement and a flexible work schedule, healthcare plans, retirement plans, life insurance, paid time off, family leave, short-term and long-term disability cover, training and development opportunities, work from home options, and a profit-based incentive.
