Clinical Applications Specialist

hace 2 días

Bogotá, Colombia Zimmer Biomet A tiempo completo

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.

As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised.

**What You Can Expect**:
**How You'll Create Impact**:
**Principal Duties and Responsibilities**:
40%
- Develop and review Case Report Form to make sure it fit study objectives;
- Devise edit checks to enforce data standards. In order to prevent data entry errors, edit checks are in place to cross checking data conflictions and misses. The edits checks are programmed according to Clinical Study Validation Rule documents.
- Performing UAT (User Acceptance Test) before study rollout.

5%
- Coordinate with business stakeholders to gather requirements, determine needs and project scope, and provide estimates for level of development effort required. The deliverables are Clinical Study Validation Rules document, as well and Clinical Data Management plan.

5%
- Establish and maintain overall system/project quality through documentation and validation of procedures and processes.

5%

15%

30%
- Review/trend Clinical data, both on granular level and study level to ensure data quality; identify training issues; and help on Risk based monitoring activity.

**What Makes You Stand Out**:

- Must have excellent communication skills, both written and verbal, and the ability to conduct professional training for internal and external staff.
- Must be detail oriented and capable of troubleshooting and resolving system irregularities and/or errors.
- Must be capable of handling confidential information.
- Must be able to work as part of a cross functional team or independently in a complex, rapidly changing environment and manage multiple projects simultaneously.
- An understanding of clinical data management functions, clinical trials, and Orthopedics is desired.
- Must possess intermediate or above skills in MS Office (Word, Excel, PowerPoint).
- Proficiency in one or more of the following programming languages is required: Java Script, PL SQL.
- Experience in Web Services, Machine learning, AI, R or SAS is a plus.
- Must be capable of learning new software packages, languages, frameworks and/or technologies as required.

**Your Background**:

- Bachelor’s degree in Information Technology, Computer Science, Data Management or related field required.
- 3-5 years of related experience required.
- B2 - C1 English

**Travel Expectations**:
EOE/M/F/Vet/Disability

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