Manager, Statistical Programming
Covance Inc
San José, Costa Rica
hace 6 horas

Job Overview :

Are you ready to discover you next career at Covance by Labcorp?

A career at Covance by Labcorp provides our employees the unique chance to create an immediate impact and difference in our patient’s lives.

will offer a rewarding career, a chance to work in an energetic & team oriented work place, and access to competitive benefits.

With the support of exceptional people from across the globe and a vast array of career options, you’ll be empowered to own your career journey with mentoring, training and personalized development planning.

Covance by Labcorp is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries.

We are recruiting for our Team in Costa Rica and we are looking to hire a Manager Statistical Programming

People Responsibilities :

I the position has full responsibility for managing or supervising a staff.

This includes hiring, coaching, scheduling / delegating work, conducting performance

reviews and determining pay / promotions. Indicate the number of direct and indirect

reports (use ranges rather than exact numbers, with the ranges for direct reports being

tighter than the ranges used for indirect reports).

C. Essential Job Duties :

Participates in proposal development for standalone, small programs and / or new drug

applications (NDAs) and in bid defense.

Actively monitors staff projects quality, timelines and budgets to foresee and correct issues

and assure project expectations are met.

Manages discretionary expenses and spending within team in order to meet budget

Work closely with leads to ensure that staff resources are used efficiently, and team is well

utilized

Manages resources within team : new hires, terminations, transfers, and contractors

Carry out line management responsibilities for assigned staff, including Performance

Management and Development activities, disciplinary procedures and administrative

activities.

Helps encourage staff career growth and development

Provides statistical programming support and technical support to team members

Act as the lead programmer overseeing technical planning for increasingly complex

projects including global and multiple study projects, ISS and ISE, and electronic

submissions.

Participates in internal and client audits, and regulatory inspections.

Proactively lead, review and amend departmental processes and documentation.

Facilitate advanced technical expertise, share knowledge at department meetings

Keeps abreast of new statistical programming practices, methods and tools, regulatory

practices, and industry trends to stimulate departmental growth

Education / Qualifications :

Recommended :

BSc, preferably in computing, life science, mathematical or statistical subject

Competencies

Cooperative, team-oriented and proactive.

Self-motivation and self-reliance. Ability to motivate others.

The ability to plan and to adapt to changing situations.

Strong delegation skills.

A professional approach at all times.

Experience : Minimum Required :

Minimum Required :

Minimum 8+ years of experience, or an equivalent combination of education or experience

to successfully perform the key responsibilities of the job.

Extensive experience and proven skills in the use of SAS® programs within a clinical trials

environment including all processes / practices used with a Statistical Programming

environment.

Knowledge in all aspects of clinical trials from initial study set-up to study completion

with an excellent understanding of the roles and responsibilities of all related disciplines,

e.g. Biostatistics and Clinical Data Management.

Strong supervisory skills, and ability to organize their own and others' work.

Strong problem solving skills, and a willingness to take ownership of decision-making.

Interpersonal and effective communication skills; able to communicate appropriately

throughout Covance and with its clients.

Good knowledge of the metrics, tools and processes used to manage projects.

Demonstrates knowledge of clinical research guidance, including Food and Drug

Administration (FDA), international regulatory agencies, international conference on

harmonization (ICH), and good clinical practice (GCP).

Reportar esta oferta
checkmark

Thank you for reporting this job!

Your feedback will help us improve the quality of our services.

Inscribirse
Mi Correo Electrónico
Al hacer clic en la opción "Continuar", doy mi consentimiento para que neuvoo procese mis datos de conformidad con lo establecido en su Política de privacidad . Puedo darme de baja o retirar mi autorización en cualquier momento.
Continuar
Formulario de postulación