Site Activation Manager - CNS - U.S. REMOTE

Who we are

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,500 experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.Join us!

What the Site Activation Manager does at Worldwide Clinical Trials

The Site Activation Manager is accountable for site activation project management and delivery activities within the CNS therapeutic area.

Responsibilities include coordination, collaboration, and oversight of site identification and central and local ECs (for NA countries only) activities, progression of essential documents collection, monitoring of investigator and site contracts status, and any other country and/or study-specific site activation tasks necessary for Site Activation in accordance with Good Clinical Practices (GCPs) and applicable local and international regulations and Standard Operating Procedures (SOPs).

May also include pre-award support by providing site activation-related input into the proposal text and budget items. Reports to a senior member of the Site Activation leadership team within the assigned therapeutic area.

What you will do

• Serve as the primary point of communication and accountability for study start-up and maintenance (if applicable) activities on assigned projects
  
• Oversee project activities of functional groups involved in site activation to ensure critical path activities are completed on time and within budget
  
• Ensure accurate compilation, management, tracking, and analysis of site activation activities in a timely manner
  
• May support feasibility and/or site identification activities, as needed
  
• Work closely with assigned team members to expedite the Site Qualification and Selection process
  
• Effectively communicate Site Activation & Regulatory (if applicable) project status to the Sponsor, GPL/CPM, and project team
  
• Prepare risk assessment and mitigation plans relating to project deliverables with input from other roles
  
• Responsible for ensuring that relevant study activities are present in the work order budget. Ensure OOS activities are tracked and captured within Change Notification Form (CNF) and follow through to execution of change order
  
• Work in conjunction with assigned project team members to develop and maintain site activation-related project plans
  
• May contribute to the development, review, and maintenance of SOPs and best practice guidelines and provide training/coaching pertaining to activities of the Site Activation department
  
• Provide input to departmental process improvement initiatives
  
• Establish and interpret site activation metrics to help drive corrective action for achieving deliverables, milestones, and/or KPIs
  
• May participate in business development activities by contributing to proposals and bid defense meetings by preparing relevant sections of proposals, budgets, and other country and/or study-specific activities related to Site Activation
  
• Report and/or escalate issues to Line Manager, Site Activation Portfolio Lead, and/or Site Activation Therapeutic Lead to ensure resolution and minimize risks to on-time deliverables
  
• Comply with SOPs, ICH GCP, and national regulations as applicable
  
• Liaise with other functional contributors and vendors as needed
  
• Perform other duties as assigned
  

What you will bring to the role

• Strong leadership and organizational management skills in planning, strategizing, managing, monitoring, scheduling, and critiquing
  
• Ability to exercise sound judgment and make decisions independently and to proactively identify and solve problems
  
• Ability to provide experience and input into initiatives relating to interacting with sites and/or customers
  
• Ability to motivate, lead, and engage a team
  
• Strong interpersonal skills in a fast-paced, deadline-oriented, and changing environment
  
• Strong oral and written communication skills to clearly and concisely present information
  
• Demonstrated ability to collaborate across the business
  
• Team-oriented work style: seeks and gives guidance
  
• Understanding of regulatory processes and guidelines
  
• Understanding of initiation, planning, and execution of clinical projects and overall project planning
  
• Awareness of ICH GCP Guidelines and the FDA/EU Clinical Trials Directives/National regulations (CTAs, Amendments, Urgent Safety Measures, End of Trial Notifications)
  
• Ability to handle multiple tasks in a fast-paced and constantly changing environment
  
• Ability to work in an organized, methodical, and self-motivated manner
  
• Proficiency in MS-Office applications including Microsoft Word, Excel, and PowerPoint; digital systems aptitude
  

Your experience

• A minimum four-year degree or nursing degree is required
  
• Minimum of 4 years CRO experience, preferably in Start-up Management, Project Management, and/or Site Management experience
  
• Proficient in cross-cultural communication
  
• Proficient in both spoken and written English
  

We love knowing that someone is going to have a better life because of the work we do.

To view our other roles, check out our careers page at Discover a world of difference at Worldwide !For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn .

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’reon a mission to hire thevery bestand 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.