Clinical Trial Manager - Rare Disease / Gen Med (Virtual)
Worldwide Clinical Trials2.8
Remote
Job details
Estimated: $71,000 - $98,000 a year
Job description
Requisition Number4946
Employment Type:Regular

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.

What Clinical Operations Site Management does at Worldwide

Clinical Trial Managers (CTMs) and Clinical Research Associates (CRAs) play a vital role in ensuring our clinical research programs are executed with the quality and excellence our sponsors expect and the care and passion patients deserve.

These roles are the backbone of every strong CRO, helping drive breakthrough scientific research and playing a lead role in every clinical trial. All CROs will promise you growth, opportunity, and maybe even a challenge. But we offer more than that. We offer an uncommon experience – one you can’t get anywhere else, with a team unlike anyone else.

At Worldwide we balance fun with the serious business of changing lives. We have a values-driven culture that is built from the ground up. We empower our team members to treat every trial like a patient’s life depends on it – because it does. Our leaders are in the trenches with you - committed to advancing science and moving mountains for our customers.

What you will do

Provide leadership and direction to clinical site management team members from study start through to closure
Serve as Site Management primary point of contact and representative for clinical monitoring and site activities within the project, including, but not limited to:
Primary Sponsor contact
Investigator and Bid Defense Meetings
Internal and External study team calls
Project-specific Audits / Inspections
Manage monitoring deliverables to achieve study budget and identify Out of Scope Activities
Oversee compliance to the Clinical Monitoring Plan, including site visits, outstanding trip reports and visit follow up letters

What you will bring to the role

Excellent interpersonal, oral, and written communication skills in English
Ability to lead and motivate a team remotely
Demonstrate initiative and problem-solving skills by offering solutions when obstacles are identified
Strong customer focus, ability to interact professionally within a sponsor contact
Proficiency in Microsoft Office, CTMS, and EDC Systems

Your experience

Bachelor’s Degree or a Nursing Degree required
1+ years’ experience as a Clinical Trial Manager, Clinical Operations Leader, Lead CRA, or equivalent role
3+ years’ experience as a Clinical Research Associate
Experience in Rare Disease required
Willingness to travel up to 30% required

Why Worldwide

At Worldwide, we balance fun with the serious business of changing lives. We have a values-driven culture that is built from the ground up. We empower our team members to treat every clinical trial like a patient’s life depends on it – because it does. Our leaders are in the trenches with you - committed to advancing science and moving mountains for our customers.

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Worldwide Clinical Trials is an equal opportunity employer, dedicated to a policy of non-discrimination in employment on any basis including age, sex, color, race, creed, national origin, religion, marital status, sexual orientation, political belief or disability.
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Company details

Headquarters

Worldwide Clinical Trials Corporate Headquarters 3800 Paramount Parkway, Suite 400 Morrisville, NC 27560

Employee

1001 to 5000

Revenue

$25M to $100M (USD)

Industry

Organization

Company Description
About Worldwide Clinical Trials Worldwide Clinical Trials is a global CRO providing full-service drug development services to the pharmaceutical and biotechnology industries across the full continuum from Early Phase and Bioanalytical Sciences through Phase II and III trials to Peri-Approval studies. At Worldwide Clinical Trials we believe successful drug development is built upon a foundation which strategically balances science, medicine, operations and commercial intelligence. Our highly consultative approach around the needs of our clients ensures that we approach every Phase I-IV drug development program as unique. Our mission is to foster the development of life changing medicines by integrating innovative methodology, rigorous science and efficient technology. The extensive medical and scientific heritage of our team combines to offer WCT clients a wealth of expertise in CNS, cardiovascular, oncology, chronic inflammatory diseases as well as many additional therapeutic areas. Our deep experience drives the knowledge, methodological rigor and expertise in linking experimental design with operational imperatives needed for the successful completion of global clinical trials. Combining our widely recognized therapeutic expertise with a robust global operations platform, we successfully manage clinical trials with our own staff across nearly 60 countries in North America, Latin America, Europe, Asia Pacific and Middle East. Our full-service capabilities enable us to meet particular trial requirements without compromising on science, safety or service. Bioanalytical/Immunoassay • Biomarker Development • Method Transfer and Validation • Pharmacokinetic Analysis and Reporting Clinical Research Services • Clinical Pharmacology • Bridging Studies • Dyna-Bridging Studies • Drug-Drug Interactions • Pharmacodynamic Modeling Clinical Development • Protocol Development • Feasibility • Project Management • Medical Monitoring • Clinical Monitoring • Site Management • Data Management • Rater Training • Biostatistics and Data Analysis • Medical Writing • Regulatory Affairs • Quality Assurance • Drug and Supply Depots • Drug Safety
Company ratings
  • Overall
    2.8
  • Company & Benefits
    3.0 / 5
  • Culture & Values
    2.7 / 5
  • Career Opportunities
    2.6 / 5
  • Work/Life Balance
    2.8 / 5
  • Senior Management
    2.5 / 5
Company reviews
"Could be great… just isn’t "
Current EmployeeSenior Scientist
Management is out of touch and performance is based on a flawed metrics system. Days are long and employees are treated terribly. Very hierarchical - not every position is valued and you’re treated accordingly. Zero room for advancement unless you start at a very low level.
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"No advancement horrible management "
Current EmployeeAssociate
Over the last 2 years the place has gone down. No advancement they take forever to fix issues with your pay. Lack of communication and if you say something you are now a target.

"Okay place"
Former EmployeeClinical Research Coordinator
This place needs a more work-life balance. Worked over 50+ hours being salary. However, would be a good company to start and grow with. Some management needs more work.

"Ambiente laboral serio pero con mucha amabilidad. Ticket comedor. Buena relación en todas las aréas"
Current EmployeeVacunadora
Muy buena empresa para adquirir experiencia. Compañerismo en todas las aréas, no importa la jerarquia. Buena predispocición de jefes y rrhh. Reglas claras de convivencia laboral. Horarios flexibles.
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