Site Activation Manager

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!

*SUMMARY: 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.

RESPONSIBILITIES:*

_Tasks may include but are not limited to: _

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 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

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

*OTHER SKILLS AND ABILITIES: *

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

*REQUIREMENTS: *

A minimum four-year college curriculum with a major concentration in medical, biological, physical, health, pharmacy, or other related science OR two-year college curriculum or equivalent education / training (nursing degree or equivalent life science degree) and experience within clinical research (e.g. CRA, Reg Affairs)
Minimum of 4 years 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

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 - $86,000.00 - $170,000.00

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.