Clinical Research Manager

Element Materials Technology

$100K — $145K *
Healthcare
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Registered Nurse with a valid Colorado license; BSN preferred.
  • Independent execution and training of clinical procedures as per protocol.
  • No disciplinary actions on license history required.
  • Clinical research experience is a plus.
  • Demonstrated team leadership with management experience preferred.
  • Strong organizational, attention to detail, and critical thinking skills.
  • Proficient in Microsoft Applications (Word, Excel, PowerPoint, Outlook).

Responsibilities

  • Lead a team of clinicians and technicians in executing complex clinical research protocols.
  • Ensure protocol compliance while managing multiple concurrent studies.
  • Track data collection and assist with participant recruitment screening goals.
  • Create and maintain case report forms and source documents.
  • Document all trial progress including adverse events and protocol deviations.
  • Manage accountability for clinical supplies and sponsor-supplied devices.
  • Communicate with sponsors and management about study design and progress.

Benefits

  • Full-time position with opportunities for career growth in clinical research.
  • Engagement in cutting-edge studies on medical devices and health technology.
  • Supportive team environment with leadership development and training opportunities.
  • Flexibility to represent the company at diverse community events.
  • A chance to work in an innovative lab setting in Louisville, CO.
Full Job Description
Overview

Element has a current opening for a Clinical Research Manager to join our growing team in Louisville, CO for a full time position. The main responsibility of the Clinical Research Manager is to act as a liaison with sponsors to oversee clinical trials of medical devices and health tech (Phases 0-2), ensuring compliance with protocols and regulatory standards and directly manage a team of clinicians.

You can learn more about the lab here: EMT Louisville CO Lab Page

Pay Range: $100k-$145k DOE

Responsibilities

  • Leads a team of clinicians and technicians in carrying out complex study protocols:
    o Management may include multiple concurrent studies
    o Studies may require multiple visits by participants
    o Studies may require travel to other states
  • Responsible for understanding protocol requirements and utilizing critical thinking skills
  • Tracks study progress in terms of data collection requirements and assists recruitment team by communicating screening goals
  • Creates case report forms, based on written protocol
  • Develops, completes, and maintains source documents
  • Documents all aspects of trial progress, including adverse events, protocol deviations, and device deficiencies; enrollment and screening logs; device accountability; and all documentation required for the Trial Master File
  • Responsible for maintaining and completing Case Report Forms in agreement with the source documentation and in accordance with the study protocols
  • Assures clinical supply accountability for assigned trials
  • Responsible for securing all sponsor-supplied devices and equipment
  • Communicates regularly with sponsors and with executive management regarding study design recommendations; study progress and status; mitigation strategies; and all aspects of the study from start to finish.
  • Has the ability to directly supervise employees that perform data analysis and clinical execution. Carries out supervisory responsibilities in accordance with the organization's policies and applicable laws.
  • Responsibilities include interviewing, hiring, and training employees; planning, assigning, and directing work; appraising performance; rewarding and disciplining employees; and addressing complaints and resolving problems.


Skills / Qualifications

  • Must be a Registered Nurse with a current license in the state of Colorado. BSN preferred
  • Ability to independently perform and also train all procedures (i.e. vital signs, laboratory tests, etc.) required by the protocol and as allowed by level of licensure and/or training
  • Must not have any disciplinary action on license history
  • Clinical Research Experience preferred
  • Ability to lead a team with clear direction, responsible delegation, goal-setting, and performance management; prior management experience preferred
  • Strong organizational and critical thinking skills, including attention to detail
  • Travel is required up to 25%
  • Must be capable of performing all clinical tasks relevant to licensure and/or training
  • Must possess excellent written and verbal communication skills
  • Must have good interpersonal skills, demonstrated through interactions with participants, Element staff, sponsor representatives, etc.
  • Proficiency in Microsoft Applications (Word, Excel, PowerPoint, Outlook)
  • Availability, flexibility, and maturity to represent the company at a broad range of events/projects in the community, with customers and within the company
  • Technical background is a plus

#LI-TK1

Similar Jobs

More Jobs at Element Materials Technology

  • Clinical Research Manager
    $100K — $145K *
    Boulder, CO 80302 (Boulder County)
    Healthcare
    In-Person
  • Clinical Research Manager
    $100K — $145K *
    Louisville, CO 80027 (Boulder County)
    Pharmaceuticals & Biotech
    In-Person
  • Quality Assurance Manager
    $80K — $110K *
    St. Paul, MN 55106 (Ramsey County)
    Aerospace & Defense
    In-Person
  • Chemist III
    $70K — $95K *
    Bend, OR 97701 (Deschutes County)
    Pharmaceuticals & Biotech
    In-Person
  • Program Manager
    $90K — $120K *
    Los Angeles, CA 90011 (Los Angeles County)
    Aerospace & Defense
    In-Person

More Healthcare Jobs

Find similar Clinical Research Manager jobs: