Worldwide Clinical Trials

Manager, Clinical Operations Site Management (Franchise Lead) - CNS - U.S. (Remote)

Worldwide Clinical Trials$112K — $222K *
US-AnywhereRemote in Research Triangle Park, NC
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Four-year degree in biological, physical, health, pharmacy, or related sciences, or equivalent education and training with ten years of experience
  • Eight years of clinical research experience as a clinical research associate
  • Two or more years of management experience
  • Extensive experience in Central Nervous System (CNS) therapeutics
  • Ability to travel and possess a valid passport

Responsibilities

  • Provide therapeutic and operational expertise throughout the program lifecycle
  • Ensure proper resource allocation for franchise projects
  • Collaborate with the therapeutic team on delivery strategies
  • Act as the main contact for the Project Management Franchise Lead
  • Present at proposal defenses and client meetings as necessary
  • Train CRAs and Lead CRAs on project specifics and compliance
  • Manage the quality of clinical work performed by the assigned team

Benefits

  • Commitment to an inclusive and equitable workplace
  • Transparent compensation practices
  • Comprehensive benefits package depending on location
  • Opportunities for professional development and training
Full Job Description
What the Franchise Lead - CNS does at Worldwide Clinical Trials

The Manager, Clinical Operations Site Management (Franchise Lead) is responsible for providing on-time and quality delivery of site management services from assigned Clinical Research Associates (CRAs) within assigned therapeutic area(s) and program(s)

What you will do

  • Provide therapeutic and operational expertise throughout the program and project delivery lifecycle
  • Ensure that projects within the franchise are properly resourced
  • Collaborate with the therapeutic team to create effective delivery strategies and solutions for franchise projects and programs
  • Act as the main contact person for the Project Management Franchise Lead
  • Present at proposal defense and client meetings as needed to support new or ongoing business
  • Ensure CRAs are trained on project specifics
  • Ensure Lead CRAs (LCRAs) are trained to support the clinical scope of work, including standard operating procedure (SOP) review, quality issue (QI)/corrective and preventive action (CAPA) understanding, and the Clinical Monitoring Plan
  • Coordinate and collaborate with Worldwide Clinical Trials Global Quality Assurance to provide training opportunities identified through CAPA information
  • Manage the quality of the assigned staff's clinical work
  • Coordinate efforts between Project Management, Site Management, and Study Start-Up
  • Establish regular communication to include quality metrics (such as site visit report compliance, source data verification metrics, and on-site metrics) and overall project "health" metrics (such as data query status, adherence to the scope of work, and resource status)
  • Conduct performance appraisals for direct reports


The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.

What you will bring to the role

  • Broad protocol knowledge; therapeutic knowledge preferred
  • Comprehensive global knowledge, awareness, and practical understanding of the biopharma industry, drug development lifecycle, and operational clinical trial delivery
  • Innovative and strategic thinker
  • Superior oral and written communication skills
  • Strong planning and organizational skills
  • Strong interpersonal skills
  • Experienced problem-solving and decision-making skills
  • Strong attention to detail
  • Understanding of clinical research principles and processes, including data collection and editing skills
  • Ability to navigate Electronic Data Capture (EDC) software such as InForm and Medidata
  • Strong knowledge of U.S. Food and Drug Administration (FDA) regulations, International Council for Harmonisation (ICH) guidelines, and the Health Insurance Portability and Accountability Act (HIPAA)
  • Understanding of standard operating procedures


Your experience

  • Four-year college curriculum with a major concentration in biological, physical, health, pharmacy, or other related sciences, and eight years of clinical research experience as a clinical research associate, OR
  • Equivalent education and training with ten years of clinical research experience as a clinical research associate
  • Two or more years of management experience
  • Extensive CNS experience required
  • Travel required
  • Passport required


Promotion to the next level is not automatic based on years of experience. Personnel are evaluated on proven competency, level of responsibility, and ability to work independently.

At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation.

The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):

United States of America - $112,000.00 - $222,000.00

The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.

About Worldwide Clinical Trials

Worldwide Clinical Trials is a global contract research organization (CRO) that provides clinical research services to pharmaceutical and biotechnology companies. They specialize in early phase development, late phase development, and full-service clinical research. Worldwide Clinical Trials has experience in a wide range of therapeutic areas, including oncology, neuroscience, and infectious diseases. They are committed to providing high-quality, efficient, and cost-effective services to their clients.
Learn more about Worldwide Clinical Trials
Size
1,500 employees
Industry
Founded
1986

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