Clinical Study Manager

Location: San Antonio, TX, USA

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Requisition Number: 5571

Position Title: Clinical Study Manager

External 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.

 

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.

 What you will do:

The Clinical Study Manager (CSM) will manage eight to ten (8-10) Phase I Clinical Trials that may be local, or regional in scope. Clinical Study Manager (CSM) is responsible for the overall coordination and management of clinical trials from start-up through closeout activities. Directs the technical, financial, and operational aspects of the projects to secure the successful completion of clinical trials.

 

The Clinical Study Manager responsibilities include, but are not limited to, the following: 

  • Lead core project team members and facilitate their ability to lead extended/complete project team
  • Lead cross-unit coordination both internal and external, inclusive of sub-contractors
  • Define and manage project resource needs in conjunction with functional heads and establish contingency plans for key resources
  • Works with functional area leads to identify and evaluate fundamental project requirements, interpret data on complex issues, is responsible for contingency planning and implementation of rescue strategy where needed and ensure solutions are implemented and ensure that all staff allocated to assigned projects are trained on the study protocol and all other study-related processes, adhere to professional standards and to SOPs as well as current Good Clinical Practice (GCP) and applicable local regulations

 

What you will bring to the role

  •  Some knowledge and skills in performing technical and laboratory procedures
  • Experience performing vital signs, ECGs, and laboratory procedures
  • Self-motivated and excellent problem-solving skills, strong interpersonal skills, ability to work independently
  • Must be able to work effectively with co-workers in a team environment and individually unsupervised.  Must be able to perform duties at a fast pace without errors.

 Your experience:

  • Required:  University/college degree (life science preferred) or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology) or equivalent combination of education and experience that provides the individual with the required knowledge, skills, and abilities

Preferred: Minimum of five (5) years of clinical pharmaceutical industry experience including demonstrated skills and competency in clinical project 

 

City:

State:

Employment Type: Regular

Community / Marketing Title: Clinical Study Manager

Company Profile:

We’re a global, mid-size CRO that pushes boundaries, innovates and invents — because the path to a cure for the world’s most persist diseases is not paved by those who play it safe, but by those who take pioneering, creative approaches, and implement them with quality and excellence. We are experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs, in the best possible way.

Location_formattedLocationLong: San Antonio, Texas US

CountryEEOText_Description: Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law. Worldwide is committed to working with and providing reasonable accommodations to applicants with disabilities. We are proud to be an equal opportunity workplace where people thrive by being themselves and are inspired to do their best work every day.

 Worldwide Clinical Trials does not accept unsolicited resumes from 3rd party vendors

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© Worldwide Clinical Trials 2021

We only accept resumes from staffing organizations with pre-approved contractual agreements. Please do not forward resumes directly to our hiring managers, jobs alias, or any other company location. Unsolicited resumes from employment agencies will not be considered and Worldwide is not responsible for any fees related to unsolicited resumes.