Senior Manager, Clinical Operations Site Management (Franchise Lead) - CNS - Europe — Worldwide Clinical Trials

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Senior Manager, Clinical Operations Site Management (Franchise Lead) - CNS - Europe

Worldwide Clinical Trials

Spojené královstvíRemotepřed 7 dny

Na první pohled

Klinický výzkumSeniorCNS trialsClinical research associateManagement experienceStrategické myšleníRemote (Evropa)

Přizpůsobit životopis

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Pošli zaměstnavateli životopis na míru během pár minut.

Přizpůsobit životopis

Koho hledáme

Broad protocol knowledge; therapeutic knowledge desired.
Comprehensive global knowledge, awareness, and practical understanding of the biopharma industry, drug development lifecycle and operational clinical trial delivery.
Innovative and strategic thinker.
Superior oral and written communication skills.
Strong planning and organizational skills.
Experienced problem solving/decision making skills.
4-year college curriculum with a major concentration in biological, physical, health, pharmacy or other related science and 8 years clinical research experience as a clinical research associate OR Equivalent education/training and 10 years clinical research experience as a clinical research associate.
At least 2 years of management experience.
Experience with CNS trials is required for this role.

Co budeš dělat

Provide therapeutic and operational expertise throughout the program/project delivery lifecycle.
Ensure that projects within the Franchise are properly resourced.
Responsible for collaborating with Therapeutic team to provide effective delivery strategies and solutions for Franchise projects and programs.
Act as main contact person for the Project management Franchise Lead.
Present at Proposal Defense/client meetings as needed to support new or ongoing business.
Ensure LCRAs are trained to support the clinical scope of work (which includes SOP review, QI/CAPA understanding, Clinical Monitoring Plan).
Coordinate and collaborate, with Worldwide Global Quality Assurance, to provide training opportunities identified in CAPA information.
Coordinate efforts between the Project Management, Site Management, and Study Start Up.
Establishing regular communication to include quality metric (SVR compliance, SDV metrics, on site metric discussion, etc.) and overall “health” of the projects (data query status, managing to the SOW, resource status).
Conduct appraisal performance review for direct reports.

O pozici

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.

Benefity

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!
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 know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. 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 .