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Clinical Research Proposal Development Jobs in Colorado

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Senior Clinical Research Associate

Denver, CO · Hybrid

$110K - $138K/yr

Senior Clinical Research Associate - Oncology Phase I - Denver, CO ICON is a global healthcare ... Atleast 2 years monitoring solid tumor clinical trials. * 1+ years early development oncology trial ...

ICON

Senior Clinical Research Associate

Denver, CO · On-site +1

$110K - $138K/yr

Senior Clinical Research Associate - Oncology Phase I - Denver, CO ICON is a global healthcare ... Atleast 2 years monitoring solid tumor clinical trials. * 1+ years early development oncology trial ...

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Senior Clinical Research Associate

Denver, CO · On-site

$110K - $138K/yr

Senior Clinical Research Associate - Oncology - West Region ICON is a global healthcare ... Learning and development opportunities through structured training and career pathways Benefits may ...

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Clinical Research Proposal Development information

What is clinical research proposal development?

Clinical research proposal development is the process of creating detailed plans for scientific studies involving human participants. This involves defining research objectives, designing study protocols, preparing budgets, and ensuring compliance with ethical and regulatory standards. The proposal often serves as a roadmap for the research team and is submitted to funding agencies or ethical review boards for approval. Properly developed proposals increase the likelihood of funding and successful project implementation.

What are the key skills and qualifications needed to thrive in clinical research proposal development, and why are they important?

To thrive in Clinical Research Proposal Development, you need a strong background in clinical research methodologies, scientific writing, and regulatory compliance, often supported by a degree in life sciences or a related field. Familiarity with grant management systems, budgeting software, and knowledge of IRB processes and funding agency guidelines is typically required. Excellent attention to detail, project management abilities, and strong interpersonal communication make someone stand out in this role. These skills are crucial to ensure proposals are scientifically sound, compliant, and competitive for funding in a highly regulated and collaborative research environment.

What are common challenges faced in clinical research proposal development, and how can I prepare to address them?

A frequent challenge in clinical research proposal development is aligning the research objectives with regulatory requirements and funding agency expectations while ensuring feasibility within timelines and available resources. Effective communication and collaboration with investigators, statisticians, and compliance officers are crucial for addressing these challenges. To prepare, familiarize yourself with funding guidelines, regulatory standards, and project management best practices, and be proactive in seeking feedback from cross-functional teams throughout the proposal drafting process.

What is the difference between Clinical Research Proposal Development vs Clinical Research Coordinator?

AspectClinical Research Proposal DevelopmentClinical Research Coordinator
Primary RoleDevelops and writes research proposals to secure funding and approvalManages and oversees the daily conduct of clinical trials at sites
Required SkillsScientific writing, regulatory knowledge, project planningPatient interaction, study coordination, data collection
Work EnvironmentResearch institutions, pharmaceutical companies, academic settingsClinical sites, hospitals, research centers
CertificationsOften requires knowledge of GCP, regulatory guidelinesOften requires GCP certification, clinical trial training

While Clinical Research Proposal Development focuses on creating detailed research proposals to obtain funding and approval, Clinical Research Coordinators handle the day-to-day management of clinical trials at research sites. Both roles require understanding of GCP and regulatory standards but differ in their primary responsibilities and work environments.

What are popular job titles related to Clinical Research Proposal Development jobs in Colorado?

For Clinical Research Proposal Development jobs in Colorado, the most frequently searched job titles are:

What job categories do people searching Clinical Research Proposal Development jobs in Colorado look for?

The top searched job categories for Clinical Research Proposal Development jobs in Colorado are:

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Cities in Colorado with the most Clinical Research Proposal Development job openings:

Clinical Research Proposal Development jobs near you

Clinical Research Psychometric Rater

Tekton Research Inc

Longmont, CO • On-site

Other

Re-posted 21 days ago

Job description

Job Description
Job Description

Position: Psychometric Rater (Full-Time/Exempt)

The Psychometric Rater will be responsible for interviewing research participants and their informants/caregivers, who are being evaluated to participate in a research study for various health conditions, in compliance with study protocol, SOPs, GCP, ICH, and FDA Regulations.

Reports to: Chief Development Officer

Job Description:

  • Reviewing the subject's medical history, meeting with potential subjects, collecting information through a prescreening interview and discussing with the Study team criteria for eligibility for a particular study.
  • Conducting a variety of psychometric rating scales on subjects with various diagnoses (such as ADHD, Alzheimer's Disease, Bipolar Disorder, GAD, Major Depressive Disorder, Post Traumatic Stress Disorder, Substance Use Disorders, Epilepsy, Anxiety Disorders, and Schizophrenia/Schizoaffective Disorder) for our clinical trials, in compliance with specific study protocols, FDA, GCP, ICH, and privacy guidelines.
  • Ability and willingness to travel to other Tekton sites to conduct ratings when needed.
  • Ensuring the subject's safety by responding appropriately to any potential for harm to self or others that are identified through the evaluations performed.
  • Working closely with other site staff and business development to promote Tekton and our sites to sponsors and CROs for new studies.
  • Attendance and presentations at conferences when needed.
  • Calculating and utilizing rating scale results as appropriate to determine protocol eligibility.
  • Meet with Sponsors, Study Monitors, and Medical Monitors as needed to address questions regarding ratings.
  • Working diligently to maintain consistency in the performance of ratings. Reviewing ratings across studies and subjects to ensure efficacy and consistency.
  • Maintaining source documentation in accordance with ALCOA-C standards and completing all monitor and sponsor queries.
  • Completing all sponsor-assigned training and meetings to obtain rater certification and re-certification per protocols requirements.
  • Attending and successfully completing all company training programs; participating in webinars and other study meetings as needed.
  • Maintaining confidentiality of subjects, customers, and company information.
  • Other duties as requested or assigned.

Required Skills/Abilities:

  • Proficiency with computer applications such as Microsoft applications, email, electronic health records, and web applications, and the ability to type proficiently (40+ wpm).
  • Strong organizational skills and attention to detail.
  • Well-developed written and verbal communication skills.
  • Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers, and external customers.
  • Ability to effectively handle multiple tasks and adapt to changes in workloads and priorities.
  • Must be professional, respectful of others, self-motivated, and have a strong work ethic.
  • Must possess a high degree of integrity and dependability.
  • Ability to work under minimal supervision, identify problems and implement solutions.
  • Ability to handle highly sensitive information

Education and Experience:

  • Master's degree in a related field is required (PhD strongly preferred)
  • 1+ years' experience performing psychometric rating scales in a clinical setting or for clinical trials, or an equivalent combination of education and experience is required.
  • Current or previous certifications to rate the following scales is highly preferred: SCID-5-CT, MINI, LSAS, HAM-A/D, C-SSRS, MADRS, MGH-ATRQ, ISI, NPI, CGI, HDRS-17, PANSS, YMRS, MMSE, ADAS-COG, CDR, RBANS, and MOCA. Bi-lingual (English / Spanish) proficiency is a plus.
  • Experience as a Clinical Research Coordinator at a research site is a plus.

Physical Requirements:

  • Prolonged periods of sitting at a desk and working on a computer
  • Must be able to lift up to 15 pounds at times
  • Ability to travel up to 50-70%


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