Live opening · Posted 21 hours ago

Senior Site Activation Manager (US)

Media Matrix Worldwide Limited · Durham, North Carolina
Workday
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At a glance

The key details from the original listing.

Posted 21 hours ago
CompanyMedia Matrix Worldwide Limited
LocationDurham, North Carolina
SourceWorkday
Listed21 hours ago

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About the role

Description supplied by the original job listing.

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 Senior Site Activation Manager does at Worldwide
This is a seasoned leadership role accountable for site activation project management and delivery activities within the assigned 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
What you will bring to the role
Proven leadership and organizational management skills in planning, strategizing, managing, monitoring, scheduling, and critiquing
Demonstrated ability to exercise sound judgment and consistently make decisions independently to proactively prevent and solve problems
Demonstrated ability to consistently and positively have an impact on initiatives relating to interacting with sites and/or customers
Demonstrated ability to motivate, lead and engage a team to consistently and successfully achieve meaningful goals
Demonstrated ability to perform and thrive in ambiguous situations
Strong interpersonal skills in a fast-paced, deadline oriented, and changing environment
Your experience
A minimum four-year college curriculum or equivalent with a major concentration in medical, biological, physical, health, pharmacy or other related science, or two-year college degree plus four years experience within clinical research
Seven years relevant CRO/pharmaceutical industry 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
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 - $107,000.00 - $213,000.00
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.
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.

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