VP of Quality and Compliance

Posted 18 Hours Ago
Easy Apply
Hiring Remotely in MA
Remote
Senior level
Cloud • Healthtech • Professional Services • Software • Pharmaceutical
We leverage technology to accelerate clinical research and bring life-changing therapies to patients faster.
The Role
The Vice President of Quality and Compliance oversees the Quality Management System, ensuring compliance with relevant regulations, and manages the Risk and Compliance Program. They collaborate with Legal and IT to maintain the Privacy Program, train staff on QMS processes, and support audit initiatives, contributing to a compliant culture within the organization.
Summary Generated by Built In

eClinical Solutions helps life sciences organizations around the world accelerate clinical development initiatives with expert data services and the elluminate Clinical Data Cloud – the foundation of digital trials. Together, the elluminate platform and digital data services give clients self-service access to all their data from one centralized location plus advanced analytics that help them make smarter, faster business decisions. 


OVERVIEW

The Vice President, Quality and Compliance is responsible for the development and management of the Quality Management System (QMS) and Compliance related CertificationsFurther this role is instrumental in management of the Risk and Compliance Program and supporting a compliant culture within the companyAdditionally, working with Legal and IT this individual helps ensure the organization Privacy Program is in line with current governing laws and regulations. and Record Retention Officer (RRO). 

KEY TASKS & RESPONSIBILITIES

  • Ownership of the QMS including Customer, Vendor, and Internal Audit Programs, QMS Related Training, and Corrective and Preventative Action Management
  • Responsible for ensuring the maintenance, support and audit of all Policies, SOPs, and Work Instructions, and that the QMS is in line with applicable company programs and regulations, such
  • Ownership of the Risk and Compliance Process along with Tracking and Trending of issues
  • Ownership of Process Training Development and Delivery for all aspects of the QMS and Regulatory areas pertinent to the business
  • Partner with Business Development, Biometrics Services, and Customer Success teams on Customer questions, RFIs, and Bid Defense activities as needed

CANDIDATE’S PROFILE 

Education/Language

  • Bachelor of Science degree in health-related field or equivalent and/or equivalent work experience along with advanced education in Business Administration or equivalent work experience preferred  
  • 20+ years’ experience in Pharmaceutical/Biotechnology industry or equivalent Senior consulting role with at least 10 years of direct Document Control and/or Quality Systems experience in a GCP setting preferred
  • 10+ years’ experience with Risk and Compliance programs across a Regulated environment preferred 
  • Excellent knowledge of English 

Professional Skills & Experience

  • Strong knowledge of ICH/GCP guidelines, 21 CFR Part 11 and clinical trial methodology
  • Strong knowledge and the ability to develop and maintain an effective of Quality Management System
  • Experience planning, performing, and hosting customer, internal, and vendor audits
  • Team leadership skills including scope management, work planning and work delegation
  • Basic negotiation, influencing, and conflict management skills to interact effectively with peers, management, clients, and vendors
  • Previous management experience required, includes hiring and retaining staff and managing remote staff
  • Self-motivated with the ability to initiate and follow through on assignments
  • Ability to work professionally with highly confidential information
  • Excellent verbal, interpersonal and written communication skills
  • Detail oriented, ability to multitask with strong prioritization, planning and organization skills

Technical Skills & Experience

  • Proficiency in Microsoft Office Applications
  • Familiarity with EDC and Clinical Data Management Systems

Accelerate your skills and career within a fast-growing company while impacting the future of healthcare. We have shared our story, now we look forward to learning yours!

eClinical is a winner of the 2023 Top Workplaces USA national award! We have also received numerous Culture Excellence Awards celebrating our exceptional company vision, values, and employee experience. See all the details here: https://topworkplaces.com/company/eclinical-solutions/

eClinical Solutions is a people first organization. Our inclusive culture values the contribution that diversity brings to our business. We celebrate individual experiences that connect us and that inspire innovation in our community. Our team seeks out opportunities to learn, grow and continuously improve. Bring your authentic self, you are welcome here!

We are proud to be an equal opportunity employer that values diversity. Our management team is committed to the principle that employment decisions are based on qualifications, merit, culture fit and business need.


What the Team is Saying

The Company
HQ: Mansfield, MA
0 Employees
Hybrid Workplace
Year Founded: 2012

What We Do

At eClinical Solutions, our goal is to leverage technology to accelerate clinical research and bring life-changing therapies to patients faster. Our industry-leading elluminate® clinical data platform is used by top life sciences companies worldwide to regain control of their data and provide meaningful analytical insights.

Why Work With Us

Our Engineering team has true greenfield opportunities for software engineers who want to develop innovative revenue-generating products that are revolutionizing the Life Sciences industry. At eClinical Solutions you can make a difference in people's lives, while having an exciting and fulfilling career.

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