Clinical Medical Coder

Are you ready for the Most Impactful Work of Your Life?
Signant Health is a global evidence generation company. We’re helping our customers digitally enable their clinical trial programs, meeting patients where they are, driving change through technology and innovations and reimagining the path to proof. Working at Signant Health puts you in the very heart of the world’s most exciting sector - a high-growth, dynamic company in an extraordinary industry. We innovate the leading-edge of clinical research data. We do it faster, better and with an eye on the future of our industry.
Role Purpose
The Associate Clinical Data Manager II is responsible for working with the Clinical Data Management team and other internal project team members to provide data management services for our customers to ensure on time and accurate deliverables. Primary responsibility of this role is to execute medical coding review and approval activities. Other responsibilities may include providing data management guidance to internal project team members and customers; communicating with internal project team members and customers on all aspects of data management activities performed for a study; authoring data management documents; performing user acceptance testing on data management deliverables; and facilitating and verifying data clarifications and data changes.
Want to join the Best Team of Your Life?
We’re looking for people who are excited by the potential to make a difference in the world. You need to be decisive, open to celebrating mistakes, able to communicate transparently and inclusively, and someone your team can count on. Most of all you need to be yourself
**As part of our team, your Key Accountabilities**:

- Execute medical coding review and approval activities.
- Works effectively within a multi-disciplinary project team to complete assigned tasks with highest level of quality, on time and within budget.
- Communicates effectively with internal project team members and customers on all aspects of data management activities performed for a study.
- Contributes to the development of data management documents (data management plan (DMP), data transfer specification (DTS), etc.).
- Contributes to UAT of reports and automated data checks programmed to support the data cleaning activities specified in the DMP.
- Verifies data extracts against the DTS.
- Provides proactive data monitoring per contractual obligations.
- Facilitates and verifies data clarifications, data corrections, and external data reconciliation.
- Actively participates in cross-functional project teams working on process improvements.

**You’ll need to bring**:
- BA/BS degree in a relevant field (Medicine, Statistics, Computer Science) or equivalent work experience.
- Strong verbal and written communication skills.
- Ability to complete high quality technical documentation and to understand requirements related to system and front-end functionality, including how that impacts how and when data is saved into the database.
- Demonstrate extreme attention to detail and organization in all aspects of work.
- Demonstrated ability to meet very short deadlines & multi-task in an extremely fast-paced work environment with little direct supervision.
- Proven ability to work both independently and in a team-oriented environment, providing back-up support to team members & establishing/maintaining effective work relationships with co-workers within and across functional areas.
- Previously demonstrated proactive and positive approach to tasks and projects overall, as well as to the types of scheduling & process changes that are inherent in a fast-paced business.
- Ability to understand requirements related to system and front-end functionality (and associated limitations) and how that impacts how and when data is saved into the database.
- Assists with other departmental initiatives and projects as required.
- Mentors less experienced staff.

We would be thrilled if you bring in the below
- 2+ years of professional experience in the clinical trials data management field.
- Experience in providing data management services in the clinical trials industry.
- Proven ability to handle multiple competing priorities in a fast-paced work environment with mínimal direct supervision.
- Knowledge of Programming Languages such as SAS, SQL, etc.
- Familiarity with 21 CFR Part 11 or experience in a regulated environment desirable.

We know that everyone has different wants and needs, which is why along with a highly competitive base salary we support our people and their loved ones with a variety of perks and benefits. As part of our team some of the benefits you can expect to receive are:

- Medical Insurance, Group Accidental Coverage/Insurance, Group Term Life Insurance
- Company Paid Subscription to Calm - The #1 app for mental fitness.
- Employee Referral Program - Bring the Best to Signant Health and earn a reward
- Wellness Program - Participate in cha