Logo for UBC

Sr Clinical Research Associate

Role overview

Qualifications

  • Bachelor’s degree – Life Science preferred or equivalent years of industry and clinical research experience
  • Minimum of 36 months on-site monitoring experience
  • Comprehensive knowledge of medical terminology and regulatory guidelines
  • Excellent critical thinking and resolution skills

Responsibilities

  • Monitors clinical trials and observational studies ensuring protocol adherence
  • Performs remote and on-site monitoring in accordance with project specific timelines
  • Completes site monitoring reports and ensures follow-up of site issues
  • Mentors and trains junior level CRAs

Key facts

Other skills

  • Mentorship
  • Critical Thinking
  • Time Management
  • Microsoft Office
  • Communication
  • Teamwork
  • Problem Solving

About the company

UBC logo

UBC

Pharmaceuticals

Dedicated to Global Product Safety, Brand Loyalty, and Patient Access Strategies that Support the Full Product Lifecycle United BioSource LLC (UBC) is a leading provider of pharmaceutical support services, partnering with life science companies to make medicine and medical products safer and more accessible. Our diverse suite of services helps bridge the gap between development and delivery and builds brand loyalty through patient access and adherence. UBC is well known for our ability to generate authoritative, real-world evidence of product effectiveness, safety, and value to assist healthcare decisions and enhance patient care. Developing a drug, taking it through commercialization, and demonstrating its post-launch value and safety is a complex journey. Regulatory hurdles and payer decision-making are increasing the complexity around drug development and product choices. UBC has aligned our expertise and industry insight to help manufacturers make informed decisions early in the product journey that ultimately optimize care and improve patient outcomes. The most successful product journeys start with great maps. UBC’s industry-leading experts work in unison to effectively navigate the product lifecycle, focusing on: Clinical Development Safety Commercialization We understand what it takes to compete in a crowded product market with many stakeholders that demand the right evidence at the right time. Our Past, Present, and Our Future UBC was founded in 2003 by industry experts with a passion for innovation and a commitment to working with pharmaceutical and biotech organizations in proving the safety, efficacy, and value of pharmaceutical and medical products. We recognized the opportunity to build an organization tailored to meet the need for scientific evidence in the healthcare industry. And, we quickly developed our core strength – the generation, analysis, and communication of real-world evidence throughout the product lifecycle.

Company details

Company typeLarge
IndustryPharmaceuticals
Company size1001 - 5000

Your match analysis

See how your profile stacks up against this role.

We compared the job requirements to your profile to show where you're strong and where you fall short.

Job description

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: YLM02H - Senior Clinical Research Associate (SCRA)

Brief Description: Monitors clinical trials and observational studies ensuring protocol adherence, managing site activities, and overseeing data collection and integrity. Ensures sites are conducting the study(ies) and reporting study data as required by applicable regulations and guidelines, and sponsor requirements. Mentors and trains junior level CRAs.

Specific job duties:

  • Thorough knowledge and application of project specific protocol
  • Performs remote and on-site monitoring in accordance with project specific timelines
  • Completes travel scheduling in accordance with project specific and UBC travel policy
  • Submits expense reports within UBC requirements
  • Attends project team meetings, department meetings and one-to-one meetings with the manager
  • Completes site monitoring reports and letters per UBC and/or sponsor SOPs requiring minimal corrections
  • Ensures follow-up of site issues and action items per UBC/sponsor timelines
  • Enters site visits, site monitoring reports, follow-up letter sent date and site contacts into UBC’s Clinical Trial Management System (CTMS)
  • Monitors within Electronic Data Capture (EDC) data entry, if applicable, and assists sites with electronic Case Report Form (eCRF) resolution
  • Reviews Investigator Site File and performs Investigational Product reconciliation
  • Maintains regular contact with assigned sites per study requirements
  • Completes all SOP review, training assessments and documentation within requested timelines
  • Assists Project Manager (PM) and management team by mentoring, training and assessing junior CRAs
  • Assists with preparation and/or delivery of presentations for UBC CRA training, departmental training and/or sponsor specific training
  • Assists PM and/or Lead CRA with additional tasks as needed
  • Travel up to 80% required in the North American region
  • Completes Site Management and Monitoring activities in accordance with project specific plans and timelines
  • Assists with other duties as assigned, which may align with other departments at UBC

Supervisory Responsibility:  None

Desired Skills and Qualifications:

  • Bachelor’s degree – Life Science preferred or equivalent years of industry and clinical research experience
  • Minimum of 36 months on-site monitoring experience including site selection, initiation, management, and monitoring activities
  • Comprehensive knowledge of medical terminology and regulatory guidelines
  • Excellent critical thinking and resolution skills
  • Excellent written and verbal communication skills in English and local language (as applicable)
  • Experience working in clinical trials and observational studies preferred
  • Experience and familiarity with CTMS, eTMF, EDC, Microsoft Office applications
  • Proven ability to deliver highly accurate work and adhere to deadlines in a fast-paced environment

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 PTO (Paid 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


Apply once. Then go straight to the hiring manager.

After you apply, unlock the direct contact details of the people who actually make the call. A quick follow-up makes you 5x more likely to land an interview.

MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
Unlocked after you apply
Β·

Research Assistant Related jobs

Other jobs at UBC

Premium

Reach out to the hiring manager directly.

Gain access to the contact details of the hiring managers who actually decide, and reach out to network with them directly. That, plus more when you upgrade:

  • Full match report with fit score and gaps
  • Career diagnostics on how recruiters read you
  • Curated company matches and warm intros
  • 48h early access to new roles

Cancel anytime.