What the Senior Site Activation Manager does at WorldwideThis 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.
