Software Testing Manager

Reposted 11 Days Ago
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Winston-Salem, NC, USA
In-Office
Senior level
Information Technology • Pharmaceutical
The Role
The Software Testing Manager oversees the Study Testing team, develops testing strategies, manages processes, and ensures quality through effective leadership and collaboration.
Summary Generated by Built In
Company Description

Founded in 2007, Clinical Ink is an innovation-driven eSource solutions company committed to making clinical research easier for sites, sponsors, subjects and regulators. Guided by a mission to eliminate paper documentation in clinical research, Clinical Ink launched SureSource® in 2011 – the company’s flagship product and the industry’s first purpose-built eSource platform designed to reduce the cost, complexity and burden of clinical research. In addition, CentrosHealth, the ground-breaking provider of configurable mobile apps for clinical trial patient engagement and electronic patient reported outcomes (ePRO) has joined Clinical Ink's suite of services creating a world-class clinical trial technology platform differentiated by its ability to conduct truly ‘paperless’ clinical trials with purpose-built solutions for pharma companies, research sites, and patients.

Job Description

Responsibilities:

• Manage and provide leadership for the Study Testing employees, including responsibility for hiring, development, performance management, coaching, counseling and termination.

• Develop and implement a testing strategy across multiple platforms including web and mobile devices.

• Design and manage a scalable testing process and system throughout growth and organizational changes.

• Act as lead during exploratory testing, bug investigation, regression testing and integration testing.

• Provide technical guidance for test designs, test development, test execution, test cycles, gap analysis, and traceability matrices. 

• Interact and collaborate with Development and Application Testing teams on an ongoing basis.

• Establish cross-functional process improvement methods to prevent redundant issues from reaching the testing phase.

• Promote a culture of quality and accountability by setting study quality goals and tracking/reporting progress across the Study Build Teams.

• Maintain subject matter expertise by studying trends in and developments in testing; participating in educational opportunities; reading professional publications; participating in professional organizations.

Qualifications

• Bachelor’s degree

• Minimum 5 years of management experience

• Fundamental understanding of proven testing techniques

• Extensive knowledge of SDLC (prefer candidates with experience in rapid release environments)

• Clinical trial lifecycle experience preferred

• Proven success in a leadership role working cross-functionally under tight deadlines

• Experience in regulated environments such as the FDA preferred

• Emphasizing excellence and attention to detail

• Positive attitude and exemplary communication and interpersonal skills.

Additional Information

Clinical Ink is an equal opportunity employer and does not discriminate against otherwise qualified applicants on the basis of race, color, creed, religion, ancestry, age, sex, marital status, national origin, disability or handicap, or veteran status.

www.clinicalink.com 

Skills Required

  • Bachelor's degree
  • Minimum 5 years of management experience
  • Understanding of proven testing techniques
  • Extensive knowledge of SDLC
  • Clinical trial lifecycle experience preferred
  • Leadership role working cross-functionally
  • Experience in regulated environments such as the FDA preferred
  • Attention to detail and communication skills
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The Company
HQ: Winston-Salem, NC
296 Employees

What We Do

Clinical ink is the global life science company that brings data, technology, and patient-centric research together. Our deep therapeutic-area expertise, coupled with Direct Data Capture, eCOA, eConsent, telehealth, neurocognitive testing, and digital biomarkers advancements, drive the industry standard for data precision and usher in a new generation of clinical trials. By harnessing digital data, we power sponsors, CROs, researchers, and patients to recenter decentralized trials and rewrite the clinical development experience.

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