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Clinical Lab Study Coordinator

Boulder, CO 80301

Posted: 02/27/2023 Employment Type: Contract Job Category: Scientific Job Number: 544899 Is job remote?: No Country: United States

Job Description


Pay 25-33/h depending on experience

Top skills/experience needed: Implement a study subject recruitment and screening plan, establish key community relationships, and ensure subject compensation.

Candidate must sit on site for this role. 

Initially it will likely be 5 days/wk, but will likely taper and become more hybrid as things are up and running smoothly.  I can’t say exactly when that will be but I expect it will not be a full-time on site position.

 Clinical Lab Study Coordinator

In this exciting role as a Clinical Lab Study Coordinator, you will have primary responsibility to manage day-to-day operations within the physiology lab. This is a coordinator role reporting to the Clinical Lab Manager. The Clinical Lab Study Coordinator will independently maintain subject recruitment, screening, scheduling and compensation responsibilities including developing and managing community outreach and laboratory advertising programs.  The Clinical Lab Study Coordinator will manage clinical study databases and assist with the drafting, distribution and tracking of study paperwork; case report forms, and informed consents and assist in the laboratory and clinical study operations through maintenance of procedures in one or more of the following areas: production, research and development, quality control/assurance, and/or compliance/environmental safety. 

A Day in the Life 

Responsibilities may include the following and other duties may be assigned. 
  • Implement a study subject recruitment and screening plan, including establishing key community relationships and ensuring subject compensation.
  • Work within the local community to develop a diverse subject pool.
  • Establish and maintain regular communication with research management and product managers
  • Develop and maintain appropriate study scheduling tools for subjects and projects.
  • Conduct laboratory support functions such as ordering, stocking, and distributing supplies and equipment, and collecting, washing, and storing equipment.
  • Maintain organizational standards: GCP, GLP, CITI training.
  • Prepare and maintain general laboratory quality controls and appropriate auditable documentation
  • Collaborate in study conduct and study subject communication, interactions, and ensure confidentiality.

Must Have (Minimum Requirements):

To be considered for this role, the minimum requirements must be evident on your resume.

Bachelor’s degree with 2 years of clinical trials/clinical research/lab experience or advanced degree with of 1 year of clinical trials/clinical research/lab experience

Nice to Have (Preferred Qualifications):
  • Advanced degree (Masters, or PhD) preferred. life sciences or related medical/scientific field or communications, marketing, or advertising. 
  • Experience in pre-market/ investigational and post market studies
  • Experience with database management, subject recruitment and consenting, data collection, and clinical reporting.
  • Knowledge and familiarity with the operations of a medical research laboratory
  • Ability to follow established guidelines/procedures for the preparation of various administrative forms, as well as learn new tasks independently.
  • Able to read and interpret technical procedures and regulatory requirements.
  • Experience in medical device clinical product trials and governing regulations.
  • Expertise with Good Clinical Practice (GCPs) and regulatory and compliance guidelines for clinical trial.
  • Proficient knowledge of clinical research study processes and study design.
  • Knowledge of data analysis techniques, including basic statistical methods

Competencies:
  • Leadership skills include strong communication, sense of urgency, high accountability, problem solving, quality focus, business integration acumen, and change management. 
  • Demonstrated ability to work effectively on cross-functional teams.
  • Experience in a high-demand and fast-paced environment. 
  • Strong problem-solving skills.

The staffing industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly and never provide banking information during the application process. Candidate safety is a top priority at Planet Pharma.

Planet Pharma and The Planet Group of Companies are equal opportunity employers. It is our practice not to discriminate against any employee or applicant based on any criteria, condition or basis protected by laws or regulations in the locations where we do business. All qualified applicants are encouraged to apply. We celebrate diversity and are committed to providing an environment of mutual respect. We believe that diversity, equity and inclusion enable us to better meet our mission and values while serving our clients across the globe. If you have a disability or handicap and would like us to accommodate you in any reasonable way, please inform your recruiter, or contact us, so that we can discuss the appropriate alternatives available.

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Although this hasn't been an issue at The Planet Group, the staffing industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly and never provide banking information during the application process. Candidate safety is a top priority at The Planet Group.

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