Associate Project Director, Clinical Assessment Training and Surveillance - UK/Europe - Remote

Worldwide Clinical Trials

Madrid

Presencial

EUR 55.000 - 70.000

Jornada completa

14 días+
Generador de candidaturas

Una candidatura completa en un minuto: currículum y carta de presentación adaptados, listos para enviar.

Supera los filtros ATS

Descripción de la vacante

Worldwide Clinical Trials is looking for a seasoned professional to manage operations in clinical trials. Responsibilities include identifying operational needs, coordinating team activities, and ensuring compliance with industry regulations.

The ideal candidate will have significant experience in global clinical trials, exceptional management skills, and a solid educational background in life sciences or business. Join us in contributing to the growth and success of clinical drug development.

Formación

  • 7+ years of clinical trial experience with at least 4 years in global trials.
  • Strong management skills and team leadership experience.
  • Excellent understanding of clinical trial operations.

Responsabilidades

  • Identify operational needs for projects.
  • Coordinate resourcing activities for awarded projects.
  • Engage in process improvement activities.
  • Review and assess budget utilization and revenue recognition.

Conocimientos

Organizational skills
Attention to detail
Interpersonal skills
Project management

Educación

Bachelor’s degree in life sciences or related field
Master’s degree or MBA

Descripción del empleo

What the Business Development Operations Department does at Worldwide

Business Development Operations is a team of highly experienced Business Development professionals who drive significant bookings targets and support Worldwide’s strategic position in a competitive market through a culture of collaboration and innovation. This tenured team supports a strong portfolio of existing business as well as being responsible for the continued significant growth of Worldwide’s future pipeline and sponsors. The team is accountable for overall sales performance, the profitable achievement of sales goals, and for aligning sales objectives with worldwide’s therapeutic and commercial strategies.

What You Will Do
  • Identify operational needs for upcoming projects, track and review current assignments for CAT Operations staff
  • Resource CAT study projects as Resource Manager
  • Engage as a Subject Matter Expert (SME) for CAT Operations activities
  • Provide operational oversight for designated CAT study projects
  • Engage in and coordinate resourcing activities for all CAT awarded projects
  • Identify training and skills gaps among staff; coordinate and assist with learning opportunities to enhance operations staff knowledge and skills of industry related regulations, processes, materials, and guidelines
  • Actively identify and engage in process improvement activities
  • Participate in QMD reviews and new QMD development
  • Author, collaborate, and review QMD documents and guidance documents
  • Coordinate and manage CAT Operations team meetings
  • Active engagement and oversight of study risk assessments, as they relate to operational activities
  • Work with department leaders to ensure alignment among CAT operational and clinical services
  • Lead and/or contribute to departmental initiatives that aim to implement policies, methods, techniques to contribute to existing service areas and department growth
  • Accountable for oversight of CAT study deliverables from Launch process to study close out
  • Assist and collaborate with Operations staff, Project Management, Contracts on vendor and study budget development, scope of work revisions, tracking and compliance
  • Assist in vendor management related concerns, including involvement with escalations, Vendor Management and Quality Assurance meetings
  • Review and assess ongoing budget utilization and revenue recognition with Operations Managers to ensure projects are meeting financial targets
  • Manage internal CAT operations meetings and other trial-specific meetings, as appropriate
  • Significant contributor to multiple strategic departmental, sponsor-related and cross-functional initiatives
  • Participate in business development activities including proposals input, capabilities, and bid defense meetings
  • Apply thorough knowledge of industry regulations and guidelines to ensure operational compliance during clinical trial conduct
What You Will Bring To The Role
  • Exceptional organizational skills, detail- and service-oriented, with excellent management / supervision skills
  • Excellent understanding of best business practices with respect to clinical trial operations and rater reliability processes
  • Knowledge and capabilities of our technology vendors and their abilities (skill) excelling in planning, managing, monitoring, and critiquing skills
  • Excellent at meeting timelines consistently and being able to effectively work under pressure
  • Continuously open to constructive, developmental feedback
  • Exceptional interpersonal skills in a fast-paced, deadline oriented, and changing environment
  • Ability to proactively identify and extend potential project issues to appropriate CAT and WCT staff
  • Basic knowledge of statistics and finance practices
Your Experience
  • Must have a minimum of a bachelor’s degree, preferably with a Master’s degree (life sciences, MBA and/or PMP certification).
  • Strong leadership, management and interpersonal skills
  • Strong planning and organizational skills
  • At least 7+ years clinical trial experience with at least 4 years’ experience in global clinical trials
  • Preferred at least 5+ years of experience managing team members or project management experience
  • Hands on experience in day‑to‑day management of all aspects of global clinical trials required
  • Prior experience in psychiatry / CNS therapeutic areas is a plus
  • The ideal candidate possesses knowledge and appreciation of all stages of clinical drug development. Effective leadership skills and a proven ability to build and foster high performance team productivity and cohesiveness is required. This position requires strong knowledge of monitoring practices, demonstrated knowledge / competence in the application of CFRs, GCPs and ICH guidelines

Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.

Consigue la evaluación confidencial y gratuita de tu currículum.
o arrastra y suelta tu archivo aquí
Similar jobs

Puestos de trabajo similares que vale la pena comparar

Associate Project Director, Clinical Assessment Training and Surveillance - UK/Europe - Remote
Associate Project Director, Clinical Assessment Training and Surveillance - UK/Europe - Remote

Worldwide Clinical Trials • Barcelona

Presencial
EUR 60.000 - 80.000
Associate Project Director, Clinical Assessment Training and Surveillance - UK/Europe - Remote
Associate Project Director, Clinical Assessment Training and Surveillance - UK/Europe - Remote

Worldwide Clinical Trials • Alicante

Presencial
EUR 70.000 - 90.000
Associate Project Director, Clinical Assessment Training and Surveillance - UK/Europe - Remote
Associate Project Director, Clinical Assessment Training and Surveillance - UK/Europe - Remote

Worldwide Clinical Trials • Elche

Presencial
EUR 90.000 - 130.000
Consultant, Clinician -Clinical Assessment Technologies- Europe- Remote
Consultant, Clinician -Clinical Assessment Technologies- Europe- Remote

Worldwide Clinical Trials • Alcalá de Guadaíra

Presencial
EUR 40.000 - 60.000
Diverse and inclusive work environment
Opportunities for career advancement
Clinician Rater, Contractor
Clinician Rater, Contractor

Worldwide Clinical Trials • Islas Baleares

Presencial
EUR 40.000 - 60.000
Senior Clinical Trial Manager - Oncology (Europe)
Senior Clinical Trial Manager - Oncology (Europe)

Worldwide Clinical Trials • Barcelona

Presencial
EUR 60.000 - 90.000
Director, Regulatory Pre-Award Strategy - Europe- Remote
Director, Regulatory Pre-Award Strategy - Europe- Remote

Worldwide Clinical Trials • Barcelona

Presencial
EUR 90.000 - 120.000
Medical Director, Medical Affairs - Neurology - Europe (Remote)
Medical Director, Medical Affairs - Neurology - Europe (Remote)

Worldwide Clinical Trials • Barcelona

Presencial
EUR 120.000 - 180.000
Associate Director, Global Clinical Operations (UK/Europe)
Associate Director, Global Clinical Operations (UK/Europe)

Worldwide Clinical Trials • Elche

Presencial
EUR 90.000 - 130.000
Site Activation Manager - Oncology - Europe (Remote)
Site Activation Manager - Oncology - Europe (Remote)

Worldwide Clinical Trials • Barcelona

Presencial
EUR 70.000 - 95.000