Headlands Research

Clinical Research Coordinator II

Headlands Research$140K — $156K *
Healthcare
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree preferred
  • Minimum 3 years of experience as a Clinical Research Coordinator
  • Medical assistant or phlebotomist certification required
  • Strong commitment to excellent customer service
  • Exceptional communication skills, both verbal and written
  • Highly organized and detail-oriented
  • Reliable and trustworthy with a professional demeanor

Responsibilities

  • Conduct research protocols ensuring integrity and compliance with guidelines
  • Manage all study aspects from planning to closeout
  • Facilitate informed consent processes and perform study procedures
  • Enter data and resolve queries related to study data
  • Manage Investigational Products and related supplies
  • Host monitoring visits and attend Investigator Meetings
  • Provide care for study patients and customer service to Pharmaceutical clients

Benefits

  • Full-time position in a stable office environment
  • Structured schedule with predictable hours
  • Opportunity to work in a compliant, quality-focused atmosphere
  • Potential for continued professional growth within the company
Full Job Description
The Role

Artemis is looking for a Clinical Research Coordinator for the San Diego office. Under the supervision of the Site Director, the Clinical Research Coordinator II is responsible for the conduct of research protocols, such that the integrity and quality of the clinical research is maintained and the research is conducted in accordance with Good Clinical Practice Guidelines. The Clinical Research Coordinator I manages study conduct from planning through study closeout.

Position Type: Full Time

Pay Range: $70,000 - $75,000/hr

Location: San Diego-no remote work

Travel: 0%

Work Schedule: Monday & Thursday - 8:30am-5pm / Tuesday, Wednesday, and Friday 7:00am-3:30 pm

Duties/Responsibilities
  • In-depth understanding of Pharmaceutical Sponsor/Industry initiated FDA studies in order to conduct the study with excellent quality
  • Managing all aspects of a study including participating in the informed consent process, coordinating and performing all visit study procedures per the protocol, entering data and query resolution, Investigational Product management, and managing all study related supplies and equipment, hosting monitoring visits, and attending Investigator Meetings
  • Providing the highest level of care for study patients and delivering excellent customer service to the Pharmaceutical clients
  • Assist with lab draws, processing and shipping


Qualifications
  • Bachelor's Degree preferred
  • Minimum three plus (3+) years of experience as a Clinical Research Coordinator required
  • Medical assistant or phlebotomist required
  • Commitment and ability to deliver excellent customer service
  • Excellent communication, punctual and responsible
  • Extremely well organized
  • Excellent verbal and written communication skills
  • Trustworthy, reliable; attentive to details
  • Mature and pleasant demeanor
  • Willingness to learn new tasks and grow with the company

About Headlands Research

Headlands Research is a clinical research company that provides clinical trial services to pharmaceutical, biotechnology, and medical device companies. The company offers a range of services, including clinical trial management, site selection, patient recruitment, and regulatory compliance. Headlands Research has a network of research sites across the United States and Canada. The company is headquartered in Princeton, New Jersey.
Learn more about Headlands Research
Size
100 employees
Industry
Founded
2018

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