← Back to jobsJob ID col-cmvgnb6vh00dd13y86f660bbu

DermCare ManagementPosted 25 days ago

Clinical Research Assistant

Full-time
On-site
Entry level
Competitive
Posted 25 days ago

Responsibilities Screening potential participants by phone and assessing their interest in study involvement Assisting with participant visit management, including administrative support during visits Scheduling participants for upcoming visits, ensuring all protocol requirements are met Sending reminders via call or text regarding upcoming visits and providing any specific instructions (e.g., fasting, bringing medic

Posted
25 days ago
Source
recruitingbypaycor.com
Sector
Healthcare

Opens the employer's application page in a new tab

Responsibilities

  • Screening potential participants by phone and assessing their interest in study involvement
  • Assisting with participant visit management, including administrative support during visits
  • Scheduling participants for upcoming visits, ensuring all protocol requirements are met
  • Sending reminders via call or text regarding upcoming visits and providing any specific instructions (e.g., fasting, bringing medication bottles, etc.)
  • Preparing for study visits by organizing materials and ensuring compliance with the study protocol
  • Managing both physical and electronic study documents, ensuring accurate filing and organization
  • Entering data from study visits into clinical trial management systems (CTMS) and secure electronic databases (EDC) as authorized
  • Performing study visit procedures as delegated by the Investigator including but not limited to vital signs, ECG, Phlebotomy, lab processing
  • Performing any additional tasks related to study operations as needed
  • Promoting a team-oriented work environment, prioritizing safety and mutual respect among colleagues
  • Complying with company policies, HIPAA, OSHA regulations, and Standard Operating Procedures (SOPs) to deliver high-quality services

Qualifications

  • High School Diploma or GED
  • Knowledge of clinical trials, industry standards, and experience with participant recruitment
  • Familiarity with medical terminology is essential
  • Ability to handle confidential information with discretion
  • Capable of working both independently and collaboratively within a team
  • Strong organizational skills, able to manage deadlines and prioritize tasks effectively
  • Basic problem-solving abilities and keen attention to detail
  • Professional and courteous phone etiquette
  • Ability to build and maintain positive relationships with internal teams and external participants
  • Creative, resourceful, and adaptable in various situations
  • Strong interpersonal skills, including tact, diplomacy, and flexibility
  • Proficiency in using computer systems and software applications
  • Willingness to continually self-educate
  • Ability to receive and process information through both oral and written communication
  • Capable of working under tight deadlines
  • Proficient in accessing, inputting, and retrieving data from a computer

Preferred

  • Bachelor's degree in a related field
  • Certification as a Clinical Research Coordinator
  • Phlebotomy experience and certification where required (highly preferred)
  • CCRC certification a plus
  • Bi-lingual in Spanish and/or Vietnamese is a plus

Required skills

Participant RecruitmentPhlebotomySpanishVietnamese

Nice to have

CCRC certification a plus

Full job description

Responsibilities

  • Screening potential participants by phone and assessing their interest in study involvement
  • Assisting with participant visit management, including administrative support during visits
  • Scheduling participants for upcoming visits, ensuring all protocol requirements are met
  • Sending reminders via call or text regarding upcoming visits and providing any specific instructions (e.g., fasting, bringing medication bottles, etc.)
  • Preparing for study visits by organizing materials and ensuring compliance with the study protocol
  • Managing both physical and electronic study documents, ensuring accurate filing and organization
  • Entering data from study visits into clinical trial management systems (CTMS) and secure electronic databases (EDC) as authorized
  • Performing study visit procedures as delegated by the Investigator including but not limited to vital signs, ECG, Phlebotomy, lab processing
  • Performing any additional tasks related to study operations as needed
  • Promoting a team-oriented work environment, prioritizing safety and mutual respect among colleagues
  • Complying with company policies, HIPAA, OSHA regulations, and Standard Operating Procedures (SOPs) to deliver high-quality services

Preferred

  • Bachelor's degree in a related field
  • Certification as a Clinical Research Coordinator
  • Phlebotomy experience and certification where required (highly preferred)
  • CCRC certification a plus
  • Bi-lingual in Spanish and/or Vietnamese is a plus

Benefits

  • Medical Insurance
  • Dental Insurance
  • Vision Insurance
  • Supplemental health benefits
  • Paid time off
  • Holidays
  • Retirement plan (401k)
  • DermCare Management is a practice management company for seasoned dermatology professionals.
  • Hollywood, Florida, USA
  • https://www.dermcaremgt.com
  • Late Stage
  • Total Funding
  • unknown
  • Key Investors
  • Oxford Finance LLC
  • 2019-10-19
  • Private Equity
  • 2019-10-10
  • Debt Financing
  • Leadership Team
  • Jeffrey Schillinger
  • Chief Executive Officer
  • Recent News
  • PR Newswire
  • PRIVACY ALERT: DermCare Management, Inc. Under Investigation for Data Breach of Patient Records
  • 2026-05-04
  • Physician Growth Partners Advises Fort Worth Plastic Surgery on Partnership with DermCare Management
  • 2026-02-25
  • Precedence Research
  • Dermatology Market to Worth USD 2.75 Billion Size by 2034

Qualifications

  • High School Diploma or GED
  • Knowledge of clinical trials, industry standards, and experience with participant recruitment
  • Familiarity with medical terminology is essential
  • Ability to handle confidential information with discretion
  • Capable of working both independently and collaboratively within a team
  • Strong organizational skills, able to manage deadlines and prioritize tasks effectively
  • Basic problem-solving abilities and keen attention to detail
  • Professional and courteous phone etiquette
  • Ability to build and maintain positive relationships with internal teams and external participants
  • Creative, resourceful, and adaptable in various situations
  • Strong interpersonal skills, including tact, diplomacy, and flexibility
  • Proficiency in using computer systems and software applications
  • Willingness to continually self-educate
  • Ability to receive and process information through both oral and written communication
  • Capable of working under tight deadlines
  • Proficient in accessing, inputting, and retrieving data from a computer
  • Bachelor's degree in a related field
  • Certification as a Clinical Research Coordinator
  • Phlebotomy experience and certification where required (highly preferred)
  • CCRC certification a plus
  • Bi-lingual in Spanish and/or Vietnamese is a plus

Required skills

  • Participant Recruitment, Phlebotomy, Spanish, Vietnamese

Preferred skills

  • Bachelor's degree in a related field, Bi-lingual in Spanish and/or Vietnamese is a plus, CCRC certification a plus, Certification as a Clinical Research Coordinator

Experience

  • Entry level

Job details

Employment type

Full-time

Seniority level

Entry level

Date posted

Oct 19, 2026

Work mode

On-site

Job source

recruitingbypaycor.com

Company

DermCare Management

Healthcare

See all 2 jobs from DermCare Management →
  • Fountain Valley, CA
  • Healthcare

Similar jobs

Other roles in Fountain Valley, CA or Healthcare

Healthcare

30+ days ago

Researcher, Agent Safety, Oversight and System Mitigations

Full-timeSan Francisco, CACompetitive

This role focuses on oversight and system-level mitigations that enable increasingly capable agents to operate safely and autonomously in real environments.

Healthcare

30+ days ago

Research Scientist - Personalization

PermanentNew York, NYCompetitive

The Personalization team makes deciding what to play next easier and more enjoyable for every listener. From Blend to Discover Weekly, we’re behind some of Spotify’s most-loved features.

Healthcare

30+ days ago

Researcher, Frontier Risk Mitigations

Full-timeSan Francisco, CACompetitive

We are seeking exceptional researchers who can push the frontier of safety mitigations. You will help derisk frontier models by developing novel safety mitigations, developing and applying new techniques from domains like interpretability, control, and…

Clinical Research Assistant

DermCare Management · Competitive

Apply on company site