Research Assistant (52908)

Platinum Dermatology Partners; Santa Ana (CA); On-site; USD 33,000 - 34,000; Full time

Benefits offered by this job

Medical Insurance

Dental Insurance

Vision Insurance

401(k) plan

Disability Insurance

Paid Time Off

Company Holidays

Employee Referral Program

Job summary

Platinum Dermatology Partners in Santa Ana, CA seeks a Research Assistant to support the Clinical Research department in screening participants, collecting data, and coordinating site activities.

This role requires a high school diploma, GCP and IATA certificates; associate degree preferred; strong organizational and interpersonal skills; experience in dermatology research is preferred.

Qualifications

• High school diploma or GED required.
• GCP and IATA certificate.
• Associate degree or equivalent experience preferred.

Responsibilities

• Answer Research department phone lines and relay messages.
• Pre-screen patients and schedule initial screenings.
• Assist with data collection, CRF completion, and document labeling.
• Maintain calibration records and temperature logs.
• Coordinate site qualification and initiation visits and assist coordinators as needed.
• Support staff with various trial-related tasks and data entry.

Skills

Excellent interpersonal skills

Ability to work in a dynamic fast pace

Strong organizational and critical-thi

MS Word, Excel, PowerPoint, Outlook

Education

GCP certificate

IATA certificate

Associate degree or equivalent experience preferred

High school diploma or GED

Tools

MS Word

Excel

PowerPoint

Outlook

Job description

Job Details

Location: Santa Ana - Santa Ana, CA 92701

Position Type: Full Time

Salary Range: $24.00 - $25.00 Hourly

Company

Platinum Dermatology Partners is a network of high-quality dermatology clinics that focus on collaborative and innovative ideas to drive growth. We offer general dermatology, cosmetic, medical, plastic surgery, and cancer screening treatments. We have over 130+ clinics, 350+ providers, and 2200+ employees in clinics across Texas, Arizona, California, Nevada, and Florida. We are a rapidly growing company that allows our doctors to focus on providing exceptional care without worrying about the operational side of the business. Our core values focus on collaboration, ownership, respect, excellence, authenticity, and integrity. Our purpose is to empower the practice of exceptional dermatology.

Company Conformance Statements

• Perform quality work within deadlines with or without direct supervision.
• Interact professionally with other employees, customers, and suppliers.
• Work effectively as a team contributor on all assignments.
• Work independently while understanding the necessity for communicating and coordinating work efforts with other employees and organizations.

Responsibilities

• Responsible for answering Research department phone lines, taking messages, and accurately relaying information to the appropriate study coordinator.
• Reads and comprehends study protocols.
• Pre-screens patients to participate in clinical trials following trial protocols and schedules initial screening appointments.
• Responds to Research web inquiries.
• Assists the Research Department and/or Clinical Research Coordinators with delegated tasks.
• Assistance with the following may be delegated but is not limited to:
  • Subject recruitment.
  • Directly collects data from the subject.
  • Maintains source documents.
  • CRF (case report form) completion and review for accuracy
  • Ensures accurate labeling of slide photos.
  • Filing and maintenance of all study-related documents.
  • Schedules study visits.
  • Documents adverse events and notifies appropriate research personnel.
  • Assist physicians, nurses, or medical staff with medical procedures.
  • Set up an exam room for specific procedures as indicated.
  • Provide patient education and literature.
  • Take pre- and post-treatment pictures.
  • Assists in cleaning rooms.
  • Monitor physician’s schedule to maintain timely flow.
  • Check voicemail and triage calls according to protocol on the same day.
  • Participates and contributes to staff meetings.
• Assist research sites when needed to collect and record data as appropriate to the specific objectives of each study.
• Assist with weekly calls with different sites to follow up on sites’ research requests and update sites’ files as needed (licenses, and training, etc.).
• Collect patient data from the database as needed.
• Assist with the collection and preparation of materials for submission to sponsors and regulations (IRB, FDA, etc.,).
• Assist with tracking requests for equipment or supplies necessary for the study.
• Assist in maintaining and updating the research website as directed.
• Assist in coordinating site qualification and site initiation visits.
• Schedule the calibration and maintain records of research equipment calibrations, as specified by the requirements of the study.
• Maintain updated temperature records.
• As assigned by the Research Director, assist coordinators in study data entry, answering queries, and during monitoring visits or Audits.
• Assist coordinators in sample processing and shipping (IATA certificate).
• May conduct patient study visits as assigned by the Research Director (GCP certificate).
• Assist in all duties of the photography room as needed (upload photos, label photos, etc.).
• Other Duties as assigned.

Education

• High school diploma or GED required.
• GCP, and IATA Certificate.
• Associate degree or equivalent experience is preferred.

Experience

• Previous Clinical Research experience preferred.
• Previous dermatology experience is preferred.
• Ability and willingness to function as part of a team.
• Ability to establish and maintain positive working relationships with physicians and providers.
• Ability to generate respect and trust from fellow employees and patients.
• Ability to show effective discretion and maintain confidentiality.
• Ability to work in a dynamic fast paced environment.
• Knowledge of spreadsheet applications.
• Possess excellent interpersonal skills to effectively communicate with patients for study recruitment.
• Ability to organize work, set priorities, complete tasks, produce high quality work, meet critical deadlines, and follow up on assignments with minimum direction.
• Excellent listening, oral, and written communication skills.
• Must be proactive and resourceful.
• Demonstrates strong organizational and critical thinking skills.
• Tactful, mature, and able to interact well with diverse personalities.
• Proficient in desktop applications such as MS Word, Excel, PowerPoint, Outlook, etc.
• Ability to operate basic office equipment such as a phone, fax, copier, printer etc.

Benefits

• Medical, Dental, and Vision insurance
• Short-term/Long-term disability
• Life and other voluntary plans
• 401(k) plan
• Employee Referral Program
• Paid Time-Off
• Company-Paid Holidays

Equipment Operated

Standard office equipment including computers, fax machines, copiers, printers, telephones, etc.

Physical Requirements

Must possess manual dexterity to operate office machines including computer and calculator; stooping and bending to handle files and supplies; and mobility to complete errands or deliveries. Includes handling of sharps and chemicals.

Equal Employment Opportunity

Platinum Dermatology Partners is committed to a policy of equal employment opportunities for applicants and Employees. Employment decisions will comply with all applicable laws prohibiting discrimination in employment, including Title VII of the Civil Rights Act of 1964, The Age Discrimination in Employment Act of 1967, the Americans with Disabilities Act of 1990, the Immigration and Nationality Act, the California Fair Employment and Housing Act, and all other applicable state and federal laws.

Platinum Dermatology Partners does not permit discrimination of any type against an employee because of any of the following legally protected characteristics: gender, race, color, religion, country of origin, mental disability, physical disability, marital status, gender identity, gender expression, ancestry, genetic information, medical condition, age, sexual orientation, or pregnancy.

Please note, that any offer of employment is contingent on the successful completion of pre-employment background checks.

No phone calls or agencies, please.

INDHP1