Central Monitoring Lead

Detalles de la oferta

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas.

With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.

Central Monitoring Lead is responsible for the execution of key Central monitoring (Site, subject & study level review as applicable) activities, and in assisting the execution of several key activities.


Central Monitoring Lead collaborates with the study team to execute Central Monitoring activities and comply with client expectations.

Central Monitoring Lead conducts review of the applicable Informatics platform and communicates findings at the country, study, site, subject level.

He / she is responsible for the conduct of central monitoring in a timely Manner. Lead to update the trial progress as per the defined plan and notify any changes / risk and escalate as appropriate.

Central Monitoring Lead may be responsible for the preparation and conduct of Central Monitoring tasks across a series of sponsor projects commencing with Informatics platform launch up to study reporting.

Minimum Required :

Minimum of 5-7 years of relevant clinical research experience in a pharmaceutical company / CRO or other equivalent experience with increasing levels of responsibility in clinical trial related roles e.

g. project management, clinical monitoring, data management and informatics.

University / college degree (life science preferred) from an appropriately accredited institution.

Recommended :
Post-graduation in Life sciences or any other applicable qualification and experience

Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials.

Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need.

Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact.


Salario Nominal: A convenir

Fuente: Kitempleo

Requisitos

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