Precision Medicine Group - Senior Manager, Data Management (LATAM)

• A minimum of 8 years of DM experience and 3 years of line management experience • Bachelor’s degree with direct clinical trial experience in a CRO or Pharmaceutical environment • Previous experience in managing people within a scientific/clinical background is preferred • Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook • Able to handle a variety of clinical research tasks • Excellent organizational and communication skills • Professional use of the English language; both written and oral • Experience in utilizing various clinical database management systems • Broad knowledge of drug, device and/or biologic development and effective data management practices • Strong leadership and interpersonal skills • Preferred: • Experience in a clinical, scientific or healthcare discipline • Dictionary medical coding (MedDRA and WHODrug) • Understanding of CDISC standards (CDASH, SDTM, ADaM, etc.) • Oncology and/or Orphan Drug therapeutic experience • Competencies • Embodies the key precision principles: Client service, purpose, accountability, mutual respect and collaboration • Ability to work independently, manage time and create plans to achieve people, revenue and business goals • Ability to work effectively with minimal direction; must be a self-motivated and self- directed individual who enjoys a challenging and dynamic work environment • Team player willing to collaborate and share knowledge • Effective leadership , communication, interpersonal and negotiation skills • Exceptional customer service orientation and proven track record of successful client relationship management • Conducts formal presentations to a wide variety of audiences including colleagues, investigative staff, and clients with a high level of proficiency • Conveys thoughts in a clear, concise, and accurate manner. Provides appropriate status on all work and projects • Embraces a standard of excellence and a rigorous adherence to laws and regulations which govern our industry • Sets a personal example of what is expected of others. Functions as an opinion leader and appropriately influences others. Willing to take informed risks within the scope of respective roles • Takes ownership of problem resolution. Adequately engages in due diligence, seeks input from others and makes informed and sound judgments as appropriate • Maintains positive relationships with colleagues. Demonstrates honesty and integrity in dealing with others. Works effectively with different types of people • Knowledge of the clinical research process from Phase I through regulatory submission • Strong knowledge of data governance, data quality, data integration, and data security principles • Proficiency in data management tools and technologies • Strong analytical and problem-solving abilities • Familiarity with data privacy and compliance regulations • Project management skills and experience in leading cross-functional teams with respect to project management • #LI-AG2 #LI-REMOTE • Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.