Lead Clinical Research Associate

Posted Yesterday
Be an Early Applicant
Hiring Remotely in US
Remote
Senior level
Biotech
The Role
Provides clinical project oversight for pharmaceutical and observational studies, managing monitoring activities, site operations, timelines, documentation, compliance, issue resolution, training, and project systems. Supports project managers with resourcing, budgets, vendors, regulatory submissions, and sponsor interactions. Maintains audit-ready eTMF and CTMS records, mentors project teams, coordinates site assignments, and may conduct site monitoring. Requires at least five years of site management experience and up to 30% travel.
Summary Generated by Built In


As a pharmaceutical support industry leader, UBC is devoted to empowering health solutions for a better tomorrow. We take pride in improving patient outcomes and advancing healthcare. At UBC we provide services to enhance the entire drug development process and commercialization lifecycle - From clinical trial support to real-world evidence generation.


Embark on a rewarding career journey with UBC! Grow your career while making a meaningful impact on the world around you. UBC fosters a culture built on our Core Values being: Collaborative, Conscientious, Curious, Consultative, and Compassionate. We believe in an inclusive workplace that fosters creativity.


If you are seeking a career that will challenge, inspire, and reward you, join us at UBC!


Job Title: YLM03H – Lead Clinical Research Associate (LCRA) 

Brief Description: Provides clinical project oversight and support to the project management (PM) team. Provides oversight and manages clinical monitoring and site management portions of projects in accordance with ICH/GCP, CFR guidelines, regional or country regulations/ legislations, as well as UBC and sponsor SOPs. 

Specific job duties:

  • Thorough knowledge of sponsor-specific project requirements, scope, protocol and timelines
  • Provides oversight of the day-to-day clinical operations of US, European and/or multi-national global projects from start-up through close-out
  • Reviews and approves monitoring reports and letters within UBC and/or sponsor timelines
  • Leads and assists with UBC and project-specific training
  • Ensures appropriate visit scheduling per protocol; tracks, reports and escalates adherence to site visit schedule, trip report metrics and documentation of completed tasks
  • Provides oversight of the issues & actions and protocol deviations to ensure timely resolution per UBC and/or sponsor timelines 
  • Serves as primary liaison for monitoring issues, escalating to PM and/or Evidence Development Operations (EDO) Manager when appropriate
  • Assists with preparation and leading of sponsor, project team and UBC meetings
  • Assists as back-up for PM and may be primary contact for UBC/sponsor interaction
  • Collaborates with PM to provide input into resourcing, analyzing cost variances, out-of-scope management, and conducting revenue recognition as applicable
  • Coordinates site assignments for team in conjunction with PM and EDO Manager
  • Monitors clinical operations aspects of the project against the established plans, SOPs and KPIs ensuring compliance
  • Assists PM with the creation and maintenance of project-specific documents 
  • Responsible for maintenance of audit-ready project systems (eTMF, CTMS, project-specific systems) as related to clinical operations
  • Mentors and supports project team 
  • May include reviewing the preparation, submission and tracking of Competent Authority (CA), Central and Local Ethics Committee and other regulatory applications, as per country requirements
  • May include oversight of contract negotiation activities with the sites as per country requirements
  • May be required to perform site monitoring as needed. 
  • May review and provide oversight of study feasibility assessments
  • May assist PM and EDO Manager with management of Vendor CRAs
  • May require up to 30% travel
  • Assists with other duties as assigned

Supervisory Responsibility: 

  • N/A

Desired Skills and Qualifications:

  • Bachelor’s degree in Health Care/Life Science preferred or equivalent industry experience 
  • Minimum of 5+ years of site management experience required with preference of 2 years field monitoring experience
  • Knowledge and understanding of the local country laws applicable to clinical trials and observational studies
  • Proficient in the operational methodologies of clinical trials and observational studies
  • Thorough knowledge of medical terminology, ICH/GCP and UBC SOPs
  • Excellent written and verbal communication skills in English and local language
  • High attention to detail
  • Excellent critical thinking and resolution skills
  • Displays leadership, organizational, communication, time management and interpersonal skills 
  • Proven skills with CTMS, eTMF, EDC, Microsoft Office, basic computer software and sponsor specific systems
  • Ability to work independently and within a cross-team environment.
  • Confident in taking responsibility for operational day-to-day project oversight
  • Ability to coordinate monitoring project activities at local, national, and international studies


Benefits:

At UBC, employee growth and well-being are always at the forefront. We offer an extensive range of benefits to ensure that you have everything you need to thrive personally and professionally. 

Here are some of the exciting perks UBC offers:

  • Remote opportunities
  • Competitive salaries
  • Growth opportunities for promotion
  • 401K with company match*
  • Tuition reimbursement
  • Flexible work environment
  • Discretionary Time Off 
  • Paid Holidays
  • Employee assistance programs
  • Medical, Dental, and vision coverage
  • HSA/FSA
  • Telemedicine (Virtual doctor appointments)
  • Wellness program
  • Adoption assistance
  • Short term disability
  • Long term disability
  • Life insurance
  • Discount programs


UBC is proud to be an equal opportunity employer and does not discriminate because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, and basis of disability or any other federal, state, or local protected class. We are committed to a diverse, equitable and inclusive culture that fosters respect for each other, our clients, and our patients.


#LI-JM1

#LI-REMOTE



Skills Required

  • Bachelor’s degree in healthcare or life sciences, or equivalent industry experience
  • Minimum 5 years of site management experience
  • Knowledge of local country laws applicable to clinical trials and observational studies
  • Proficiency in clinical trial and observational study operational methodologies
  • Thorough knowledge of medical terminology, ICH/GCP, and company SOPs
  • Excellent written and verbal communication skills in English and the local language
  • High attention to detail
  • Strong critical thinking and issue-resolution skills
  • Leadership, organizational, communication, time management, and interpersonal skills
  • Proficiency with CTMS, eTMF, EDC, Microsoft Office, basic computer software, and sponsor-specific systems
  • Ability to work independently and in a cross-team environment
  • Ability to take responsibility for day-to-day operational project oversight
  • Ability to coordinate monitoring activities for local, national, and international studies
  • At least 2 years of field monitoring experience

UBC Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about UBC and has not been reviewed or approved by UBC.

  • Flexible Benefits — Pay and benefits are framed as role- and location-dependent, with flexibility (including remote/hybrid options and discretionary/enhanced time off) repeatedly positioned as a meaningful part of the total rewards value.
  • Healthcare Strength — Health coverage is described as broadly comprehensive in multiple places, including medical/dental/vision and life/disability elements, with additional support like EAP/wellness initiatives included in the total rewards framing.
  • Retirement Support — Retirement support is repeatedly present as a defining benefit component, with a 401(k) and company match frequently cited as a notable part of the package.

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The Company
HQ: King of Prussia, Pennsylvania
2,365 Employees

What We Do

United BioSource LLC (UBC) is the leading provider of evidence development solutions with expertise in uniting evidence and access. UBC helps biopharma mitigate risk, address product hurdles, and demonstrate safety, efficacy, and value under real-world conditions. Underpinned by our scientific expertise, data and analytics, and innovative technologies, we offer our customers flexible solutions generating the relevant real-world data necessary to make more informed decisions earlier, meet stakeholder requirements, and ultimately, drive better patient outcomes.

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