Senior Manager, Data Management – LATAM

🕒 May 22

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Precision Medicine Group

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 2012

🧬 Biotechnology

⚕️ Healthcare Insurance

💊 Pharmaceuticals

💰 $35.2M Venture Round on 2021-03

Biotechnology • Healthcare Insurance • Pharmaceuticals

Precision Medicine Group is a global team of experts that specializes in precision medicine, which combines advanced lab sciences, translational informatics, regulatory affairs, payer insights, and marketing communications. The company focuses on overcoming product development and commercialization challenges for pharmaceutical and life sciences clients. Their services include biomarker-driven research and development, as well as commercialization support for life science organizations from launch to product maturity. Precision Medicine Group operates through two main arms: Precision for Medicine and Precision AQ, specializing in clinical and commercial solutions respectively.

📋 Description

• Manage the day-to-day activities of the Data Management (DM) function in accordance with Standard Operating Procedures (SOPs) • Responsible for the successful planning, implementation, and execution of DM contracted activities • Provides oversight to data management projects, coordinating inter-departmental and client communication • Supports the Head of Department in functional training, hiring, defining standards, and executing department goals • Acts as the point of contact for internal team and sponsors, ensuring timely task performance • Manages, directs, leads, develops, and supervises data managers • Reviews RFPs, proposals, and related project estimates • Oversees project data entry processes and ensures adherence to project timelines • Responsible for ensuring data quality and timeliness of DM deliverables are met and aligned with business goals • Oversees completeness of data management documentation for the Trial Master File • May liaise with third-party vendors supporting timelines and data-related deliverables.

🎯 Requirements

• 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.

🏖️ Benefits

• May require some domestic and international travel