Director, Operational Strategy

hace 2 semanas

Bogotá, Bogotá D.E., Colombia Labcorp A tiempo completo

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.


Did you know?
We are looking in Latin America a Director Operational Strategy & Planning in the Oncology unit.

For this role we are looking an experience and flexible professional

Essential Job Duties:


Using an evidence-based approach, work with relevant business development staff and operational leaders to design innovative, but practical and fiscally responsible strategies for inclusion in relevant business development documents and for use in the successful implementation and conduct of clinical trial programs for clients.

Senior regional contact for both internal staff and clients for matters pertaining to OS&P.
Effectively network with others throughout Covance to ensure relevant input to project strategies and associated planning activities occurs.

Engages with project teams at key time points in the project lifecycle to ensure actual performance is in line with strategic plan and provides advanced interventional guidance when required.

Remain current with industry innovations and advances so as to include relevant advances and technology into the design of trial strategies.

Line management responsibility for the recruitment, training, utilization, development and performance review of assigned personnel. Supervises others in CDS Clinical Informatics across the Latin America region.

For this Role we will need someone with


Minimum of eight (8) years relevant clinical research experience in a pharmaceutical company/CR0, including at least five years of full project management responsibility.

Very strong technical writing skills and analytical skills
Strong networking abilities and an ability/willingness to work with individuals across the globe
Excellent communication, planning &organizational skills
Ability to inspire, to lead by example and motivate teams to seek solutions and get results
Strong abilities to negotiate and liaise with customers in a professional manner
Thorough experience in end to end (full service) clinical trial management, ideally with global
project management experience
Abilities to review/analyze relevant data so as to build evidence-based strategies.

Abilities to design/develop effective strategies to bring about trial success, as defined by clients and project teams through the use of an evidence-based approach.

Strong computer skills with an ability to understand and access and leverage technology alternatives.
Ability to work independently
Demonstrated ability to handle multiple competing priorities effective.

Education/Qualifications/Certifications and Licenses

Minimum Required:
University/College Degree (preferably postgraduate degree)
Thorough understanding of global drug development and the clinical trial project management process.

Thorough and practical working knowledge of ICH-GCP Guidelines, including relevant international requirements/guidelines for the conduct of global clinical development programs.


Preferred:
An understanding of aspects surrounding Covance business development (time and cost estimates, bid defense, contracts)
An understanding of Covance procedures, including Standard Operating Procedures.

Labcorp is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind.

We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic.

We encourage all to apply.

For more information about how we collect and store your personal data, please see our Privacy Statement.

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