Job Description
How will you make an impact?
The Senior Clinical Data Manager II is responsible for study Data Management activities from study start up to close out. The Senior Clinical Data Manager II creates the data cleaning strategy and leads the data cleaning efforts supporting Clinical Studies. The Senior Clinical Data Manager II works with Data Management, Biostatistics and Clinical Operation teams to develop standard operating processes in support of clinical research. The Senior Clinical Data Manager will mentor junior team members and may take on more complex studies or studies in new indications.

What will you do?

Project Management:

• Represent Data Management in study team meetings, providing data status metrics and providing guidance on issues related to data management.
• Responsible for study Data Management activities from study start up to close out.
• Author Data Management timelines for assigned studies.Manage performance, quality, and timeliness of data from service providers (e.g., Central Reading Centers, Labs, Medical Coders).

Team Leadership:

• Mentor junior clinical data managers.
• Foster a collaborative and high-performance team culture.

Data Management Documents:

• Author Data Management documentation (e.g. Data Management Plans, Data Review Guidelines and eCRF Completion Guidelines, and Study Timelines, etc.)
• Author Data Management training materials used for Investigator Meetings, in-house personnel, and site staff.
• Maintain Data Management project documentation including vendor files in an audit- ready manner.
• Assist the Lead Clinical Programmers with the creation and maintenance of Data Transfer Agreements.

Data Review:

• Lead and perform regular data review across Glaukos studies to identify quality issues, data trends/outliers and generate queries as necessary.
• Review and reconcile data from external sources.

Database Build and User Acceptance Testing (UAT):

• Assist with the creation of the CRF and Edit Check Specifications documents.
• Perform User Acceptance Testing (UAT) of clinical databases including EDC.

EDC User Management:

• Manage EDC User Access for all assigned studies.

Collaboration with Cross-Functional Teams:

• Provide ongoing day-to-day support to the Clinical Study Teams to ensure all data is reviewed and discrepancies are resolved.
• Collaborate with internal team and stakeholders to ensure deliverables meet timelines.
• Work with Clinical Programming to produce additional reports outside of the Data Review Guidelines to facilitate efficient data review and cleaning.
• Facilitate cross-functional Data Management meetings and discussions with Study Managers, Clinical Study Teams, Project Managers, Programming and Regulatory.
• Generate reports or data listings for study teams as needed.
• Serve as a clinical data management expert, understand industry best practices, and provide input to the clinical team.
• Review Protocol and provide feedback to the Clinical Study Team on data collection related items.

Process Improvement:

• Participate in the review and update of the Data Management standard operating procedures, work instructions, and templates.
• Participate in the development of departmental processes and procedures.

How will you get here?

• Minimum of 8 years of experience working in clinical data management, preferably in the pharmaceutical or medical device industry.
• Understanding of clinical trial process.Understanding of FDA/ICH guidelines and industry/technology standard practices.
• Understanding of Good Clinical Data Management Practices (GCDMP) and other regulatory guidelines specific to data management.
• Proficient in using Electronic Data Capture (EDC) systems (e.g. MedNet, Rave, Veeva Vault EDC, etc.).
• Proficient at reviewing data using various data using various reporting and analytic tools.
• Multi-tasking, problem-solving and verbal and written communication skills essential.
• In depth Project Management experience.Proficient in writing Data Management documentation (e.g. Data Management Plan, Data Review Guidelines, and eCRF Completion Guidelines, and Study Timelines, etc.).
• Experience in creating Case Report Forms and Edit Check Specifications.Excellent verbal and written communication skills.
• Ability to work well with others.Understanding of CDISC Standards (CDASH, SDTM).
• Ability to effectively manage a variety of data management tasks for multiple clinical studies and different stages of activity.
• Flexibility in responding to change or business needs.
• Proven ability to preemptively identify data and system issues and mitigate risks to data quality.
• Bachelor's degree in a relevant scientific or technical discipline.

Desirable

• Familiarity with Ophthalmology Therapeutic area.

Generous. Innovative. Leadership-driven. Family-oriented. Socially responsible.
These are just a few of the terms our employees use to describe their experiences as a part of the Glaukos family.
Those may seem like big aspirations, but here at Glaukos, we recognize the deep significance and profound meaning that comes from knowing that we can make a meaningful difference by helping improve eyesight of people worldwide. And because we're a rapidly growing company with a dynamic, fast-paced culture, individual employees are empowered with more diverse and enriching challenges that might not be possible at a larger company, and more fulfillment in knowing every person and every task is directly tied to making a difference in the life of others.
We offer competitive salary (based on experience), bonus eligibility, medical/dental/vision, life insurance, stock options, 401(k) Employer Match, Employee Stock Purchase Program, generous time off & paid holidays as well as time-off to volunteer in the community, plus the opportunity to work for a company that is pioneering a new glaucoma treatment class! Moreover, Glaukos Corporation has been Certified as a Great Place to Work the last three years!
Glaukos Corporation is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.

#GKOSUS

About Us
Generous. Innovative. Leadership-driven. Family-oriented. Socially responsible.

Founded in 1998, Glaukos Corporation is an ophthalmic pharmaceutical and medical technology company focused on developing and commercializing novel therapies for the treatment of glaucoma, corneal disorders, and retinal diseases.

Our mission at Glaukos is to truly transform vision by pioneering novel, dropless therapies that can meaningfully advance the standard of care and improve the lives of patients suffering from chronic, sight-threatening eye diseases.

Innovation is at the core of everything we do, and we are resolute in our commitment to challenge conventional thinking with new treatment alternatives that are supported by real science, robust clinical evidence, and an unrelenting focus on patients.

Our constant pursuit of game-changing technologies that disrupt legacy treatment paradigms is encapsulated in the Glaukos mantra "We'll Go First," which articulates our willingness to take chances, our determination to forge new ground, and our commitment to continuous improvement in all that we do.

Our company completed an initial public offering in June of 2015, and our shares are traded on the New York Stock Exchange under the ticker symbol "GKOS". Our global headquarters is in Aliso Viejo, California with additional locations in San Clemente, California, and Burlington, Massachusetts.

Glaukos Corporation is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.