RTSM Specialist (US/CA) 12 month contract

Worldwide Clinical Trials; Durham (NC); On-site; USD 72,000 - 143,000; Full time

Job summary

Worldwide Clinical Trials in the United States is seeking an RTSM Specialist to manage the successful implementation of RTSM systems from award to decommissioning, within time and costframes. You will lead study design, URS reviews and coordinate cross-functional teams across sponsor study groups and vendors.

Responsibilities include budget oversight, project communications, and ensuring delivery on milestones; travel may be required to Investigator Meetings and related events.

Qualifications

• Educated to degree level in a relevant discipline or able to demonstrate equivalent experience.
• Minimum 2 years prior RTSM experience.
• Minimum 1 year prior project management experience.
• Minimum of 5 years experience within CRO/pharma environment.
• CRO or Pharmaceutical experience required.
• Familiar with RTSM topics, including RTSM study design, randomization methodologies, and just-in-time drug supply.
• Understanding of clinical trials, blinding, patient safety, data integrity and associated regulations.
• Proven ability to manage delivery of RTSM solutions deployed in clinical trials.

Responsibilities

• Provide project management oversight from award to RTSM decommissioning, including oversight and accountability of deliverables and timelines.
• Communicates information on RTSM project activities to stakeholders, including sponsor study teams; serves as escalation point.
• Coordinate and deliver RTSM project communications, including status reports, agendas, minutes and calls.
• Willingness to travel and attend Investigator Meetings or other project-related meetings as required.
• Responsible for RTSM project budget and ensuring accurate vendor work orders.
• Oversee RTSM study design and URS review/approval.

Skills

English communication

Client-facing

Office software

Attention to detail

Prioritization

Education

Degree in a relevant discipline

Job description

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 RTSM Specialist Does At Worldwide

Manages the successful implementation of assigned RTSM systems or amendments in accordance with the client's requirements, within the time and cost frameworks agreed upon and to Worldwide company standards.

What You Will Do

• Provide project management oversight from award to RTSM decommissioning, including oversight and accountability of deliverables and timelines and completion of work to Worldwide SOP standards
• Communicates information on applicable RTSM project activities to stakeholders, including internal and sponsor study teams. Serves as the escalation point of contact for all RTSM assigned study-related project issues
• Overall accountability for coordination and timely delivery of RTSM project communications including study status reports, meeting agendas and minutes and scheduling project calls
• Willingness to travel and attend Investigator Meetings or other types of project related meetings when required
• Responsible for overall RTSM project budget and ensuring accurate vendor work orders for assigned studies
• Responsible for overall RTSM study design, as well as writing or reviewing and approving User Requirements Specification (URS)

What You Will Bring To The Role

• Ability to communicate concisely and effectively in both written and spoken English
• Proficient client-facing skills
• Proficient in the use of common office software
• Self-motivated individual who can positively contribute to a team environment
• High attention to detail
• Ability to prioritize and handle multiple projects simultaneously

Your Experience

• Educated to degree level in a relevant discipline or able to demonstrate equivalent experience
• Minimum 2 years prior RTSM experience
• Minimum 1 year prior project management experience
• Minimum of 5 years experience within CRO /pharma environment
• Contract Research Organization (CRO) or Pharmaceutical experience required
• Familiar with RTSM topics, including RTSM study design, randomization methodologies, and just-in-time drug supply
• Understanding of clinical trials, blinding, patient safety, data integrity and associated regulations
• Proven ability to manage delivery of RTSM solutions deployed in clinical trials

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 - $71,500.00 - $142,500.00

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.