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Sr. Clinical Research Project Manager - Remote

5+ years
$95,045 to $115,000 per year
10 July 31, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Sr. Clinical Research Project Manager

Company: CPC Clinical Research
Location: Remote

Apply Now: Sr. Clinical Operations Manager Position

Are you an organized and adaptable professional who can balance strategic vision with day-to-day tasks? If so, we want to hear from you!

Role Overview:

As a Sr. Clinical Research Project Manager at CPC Clinical Research, you will serve as the primary point of contact for industry-sponsored clinical trials, Endpoint and Specialty Services activities, and other assigned projects. This role involves overseeing clinical operations, mentoring Clinical Operations Managers, and ensuring the quality and efficiency of project services.

General Responsibilities:

  • Leadership: Collaborate with the Head of Research and Community Health Operations and the Head of Endpoint and Specialty Services to ensure high-quality project services and proactive issue resolution.
  • Mentoring: Provide guidance to Clinical Operations Managers on project management practices and deliverables.
  • Site Management: Oversee site activities for single-site or smaller multi-center studies, including site identification, evaluation, initiation, and monitoring.
  • Documentation: Manage regulatory document collection, IRB submissions, and development of essential project documents.
  • Project Management: Define and monitor project scope, timelines, and deliverables, and contribute to process improvements.
  • Training and Oversight: Identify and ensure completion of project-specific training, oversee trial-related activities, and provide performance feedback.
  • Vendor and Contract Management: Develop and manage contracts, including those for investigational products and clinical services, and oversee vendor services.

Endpoint and Specialty Services Responsibilities:

  • Scope Management: Define and monitor Endpoint and Specialty Services scope and deliverables.
  • Safety Plans: Oversee SAE processes and execution of safety plans.
  • Data Management: Ensure accurate tracking and processing of Endpoint and Specialty Services documents and data.

Qualifications:

  • Education: Nursing or BA/BS in a scientific field or equivalent experience.
  • Experience: 5 years in a clinical research setting and 3 years in sponsor or CRO clinical research project/operations management.
  • Skills: Demonstrated ability in trial management, mentoring, knowledge of Good Clinical Practice (GCP) guidelines, and proficiency in Microsoft Office.
  • Communication: Excellent organizational and communication skills with great attention to detail.
  • Travel: Willingness to travel 20-25%.

Compensation and Benefits:

  • Salary: $95,045 - $115,000 annually.
  • Benefits: Comprehensive package including medical, dental, vision, life insurance, STD, LTD, matching 401(k) plan, paid holidays, vacation days, sick time, and more.
  • Additional Perks: In-suite exercise and relaxation room, monthly team-building events, and flexible remote work options.

About CPC Clinical Research:

CPC Clinical Research is a leading academic research organization with over 30 years of experience in clinical trial design and management. We specialize in cardiovascular, wound healing, diabetes, and other therapeutic areas, and focus on innovative community health programs.

Learn more about us and our values at: CPC Clinical Research

Equal Opportunity Employer: CPC provides equal employment opportunities without regard to race, color, sex, sexual orientation, gender identity, national origin, disability, military status, or any other protected status. For assistance, email our HR team at careers@cpcmed.org.

Apply now to join a dedicated team making impactful advancements in clinical research!