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WORK WITH US

FOMAT & DRS are places where people are proud to work, have the opportunity to develop their careers and are enabled to realize their full potential. We are a therapeutically focused site management organization with a high performance reputation for conducting global clinical development programs of the highest integrity.

We are one of Latin America’s largest SMOs for Phase I – Phase IV Clinical Trials, in terms of sites & quality results. Our size and scope permit our employees to experience working in various countries and cultures on projects for top pharmaceutical companies, biotech startups, and everything in between.

Clinical Coordinators are responsible for organizing and overseeing the administrative aspects of health services and hospital departments. They work in hospitals, clinics, academic medical programs, and other patient care environments. Among their daily duties, a clinical coordinator may plan budgets, oversee personnel hiring and training, schedule staff, manage supplies and inventory, and create and evaluate long-term programs and strategy for a hospital department.

 

Task and Responsibilities:
Coordinates inventory, order processing and distribution of products and services.
Manages paperwork, electronic correspondence, and data. 
Ensure subject safety by providing information regarding adverse events and any pertinent information
to subjects and investigators in a prompt manner.
Assist the principal investigator to assure that only qualified individuals perform study related procedures
with appropriate level of supervision under the laws of the state.  

Education and Experience: 
B.S. or B.A. (preferably in the Life Science field) or an equivalent combination of education and experience.
Medical device or drug related clinical experience.
Must have analytical skill, be detail oriented and have good interpersonal skills.

Skills and Competencies:
Excellent written and verbal communication skills.
Ability to prioritize multiple timelines and task.
Ability to communicate at all levels of an organization.
Skilled with PC and Microsoft office.
Flexible and able to work in fast paced environment.
Team player.

Physical Requirements:
Some travel may be required for networking and education purposes.

Position Available in the following Locations:
Guayaquil, Ecuador 
Quito, Ecuador
Bogota, Colombia
Lima, Peru
Oxnard, California, USA

A Medical Coordinator is a licensed physician who implements and evaluates health projects, and monitors their progress to identify and rectify problems. They must remain well informed of all policies and procedures as they relate to each project, and work extensively with key directors and management personnel. Communicating with a wide range of health care authorities and other medical coordinators is imperative to achieve mutual goals.

 

Task and Responsibilities:
Coordinates inventory, order processing and distribution of products and services.
Manages paperwork, electronic correspondence, and data. 
Ensure subject safety by providing information regarding adverse events and any pertinent
information to subjects and investigators in a prompt manner.
Assist the principal investigator to assure that only qualified individuals perform study related procedures
with appropriate level of supervision under the laws of the state.  

Education and Experience: 
M.D. or an equivalent combination of education and experience.
Medical device or drug related clinical experience.
Must have analytical skill, be detail oriented and have good interpersonal skills.

Skills and Competencies:
Excellent written and verbal communication skills.
Ability to prioritize multiple timelines and task.
Ability to communicate at all levels of an organization.
Skilled with PC and Microsoft office.
Flexible and able to work in fast paced environment.
Team player.

Physical Requirements:
Some travel may be required for networking and education purposes.

Position Available in the following Locations:
Guayaquil, Ecuador 
Quito, Ecuador
Bogota, Colombia
Lima, Peru
Oxnard, California, USA

The Clinical Project Manager is charged with managing and executing clinical studies from study initiation through study closeout, as well as assuring compliance with regulatory and quality procedures and standards. Furthermore, accomplishes project objectives by planning and evaluating clinical research project activities.

Education and Experience: 
B.S. or B.A. (preferably in the Life Science field) or an equivalent combination of education and experience.
Medical device or drug related clinical experience.
4-6 years of medical device or drug related clinical experience
 (with a minimum of 2 years of experience in project management).
Must have analytical skill, be detail oriented and have good interpersonal skills.

Responsibilities:
Work with Regulatory Affairs to manage US and international regulatory submission 
for the conduct of clinical studies and the approval of new products.
Manage CRO and/or other outside clinical Vendors.
Manage Study timelines and budgets.
Drive clinical study communication and marketing initiatives.
Coordinate and supervise study execution and contract management for usability and user preference studies.
Support other clinical activities within the department as needed.

Skills and Competencies:
Excellent written and verbal communication skills.
Ability to prioritize multiple timelines and task.
Ability to communicate at all levels of an organization.
Skilled with PC and Microsoft office.
Flexible and able to work in fast paced environment.
Team player.

Physical Requirements:
Some travel may be required for networking and education purposes.

Position Available in the following Locations:
Oxnard, Ca.