Revance Therapeutics

Clinical Research Scientist

Revance Therapeutics$90K — $120K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree with 3+ years of directly related experience.
  • Preferred degree in Science, Engineering, or Food Science with a Dermatology focus.
  • Experience in pharmaceutical, medical device, cosmetic, or consumer product research.
  • Hands-on experience in clinical and consumer methodology, protocol development, and questionnaire design.
  • Proficiency in statistical analysis and report writing.

Responsibilities

  • Ensure studies comply with protocols and regulations.
  • Recruit and screen study participants; perform intake assessments.
  • Create and maintain study documents and records.
  • Manage inventory of study-related equipment and supplies.
  • Liaise with study participants, addressing inquiries and providing updates.
  • Collect specimens and enter data into electronic systems.
  • Lead research studies, adhering to protocols and standards.

Benefits

  • Flexible PTO, holidays, and parental leave.
  • Generous healthcare benefits including HSA match and 401k match.
  • Employer-paid life and disability insurance, as well as pet insurance.
  • Wellness discounts and a variety of other benefits.
Full Job Description
Job Summary:

The Clinical Research Scientist develops, designs, and executes clinical and consumer research studies to assess the efficacy and consumer appeal of selected Revance products and technology. Communicates study results regarding clinical and/or consumer findings as well as makes claim-related recommendations to various departments.

Reporting to: Clinical Research Manager
Location: Dallas, TX - onsite

Responsibilities/Essential Duties:
  • Responsible for ensuring study is in compliance with study protocol, local and federal laws, and regulations.
  • Recruits and screens potential study participants and performs intake assessments, and follows up with study participants.
  • Creates and/or maintains all documents and records related to the study, including source documents.
  • Maintains the Regulatory Binder for each Research Study.
  • Acts as point of reference for study participants by answering questions and keeping them informed on the study progress.
  • Manages the inventory of equipment and supplies related to the study and orders more as needed.
  • Attends meetings, events and seminars in order to promote the study.
  • Able to consent study participants per ICH GCP guidelines.
  • Responsible for liaising and supporting all Recruitment efforts of internal and external sources.
  • Collects specimens and inputs data and patient information into electronic systems.
  • Creates reports on each study, including notes on protocols, data collection, and more.
  • Completes visits with study subjects and schedules follow-up.
  • Collaborates closely with the Investigator and clinical staff in scheduling future appointments, explaining patient diairies, questionnaires, reporting of adverse events, recognizing serious adverse events.
  • Acts as a lead on research studies and completes all study related procedures per protocol.
  • Takes ownership of creating presentations related to study progress.
  • Responsible for preparing Research charts and Regulatory binders for monitoring and audits.
  • Adheres to ethical standards.
  • Performs miscellaneous job-related duties as assigned.

Basic Qualifications:
  • Bachelor's degree & 3+ years' directly related experience.

Preferred Qualifications:
  • Bachelor's degree in Science, Engineering, or Food Science/Technology with a Dermatology Clinical emphasis.
  • 3 years' related experience in pharmaceutical, medical device, cosmetic, consumer product, or food industry research.
  • Exposure with hands-on experience to clinical, bioinstrument, consumer methodology, protocol development, and questionnaire design in these areas.
  • Advanced certification, degree or extensive experience in clinical evaluation and/or consumer use testing.
  • Demonstrated a proficiency in protocol and questionnaire design and conduct of clinical and consumer product research analysis and report writing.
  • Solid understanding of both clinical, consumer/market research evaluation and an understanding of the relationship to the diverse Revance product areas.
  • Understand and apply strong math skills such as computing summary statistics (averages, means, median, and mode) and percentages, rations, and frequency distributions.
  • Demonstrated a proficiency at basic level statistical analysis.
  • Demonstrated proficiency in Microsoft Office programs (Word, Excel, & PowerPoint).

What Revance invests in you:
  • Competitive Compensation including base salary and annual performance bonus.
  • Flexible PTO, holidays, and parental leave.
  • Generous healthcare benefits, HSA match, 401k match, employer paid life and disability insurance, pet insurance, wellness discounts and much more!

About Revance Therapeutics

Revance Therapeutics is a biotechnology company focused on developing and commercializing innovative products for aesthetic and therapeutic applications. The company's lead product, DaxibotulinumtoxinA for Injection, is a novel botulinum toxin that has the potential to be a best-in-class product for the treatment of glabellar lines and other aesthetic and therapeutic indications. Revance Therapeutics was founded in 2002 and is headquartered in Newark, California.
Learn more about Revance Therapeutics
Size
495 employees
Market Cap
$1.5 billion
Industry
Net Income
-$282 million
Founded
2002
5 Year Trend
+203.9%
Revenue
$15.3 million
NASDAQ

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