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Careers in Brazil
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| Research Associate I |
Provides administrative support to Project Managers, Clinical Research Associates, and other clinical administration staff under the
direction of an assigned Project Manager.
Works with assigned clinical research teams to assist in reaching desired project and team goals within project timelines.
Requirements:
Excellent English and grammar skills.
Minimum 1 year administrative support experience.
Excellent Microsoft Word and Excel skills.
Excellent computer, typing and data entry skills.
Self-motivated and ability to contribute to a positive workplace.
Strong communication and interpersonal skills.
Excellent organizational skills and strong attention to detail, with proven ability to handle multiple tasks effectively.
Ability to work with project teams. |
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| Clinical Research Associate I |
Performs and coordinates all aspects of the clinical monitoring process in accordance with GCPs and global SOPs to assess the
safety and efficacy of investigational products and/or medical devices. Conducts site visits to determine protocol and regulatory
compliance, and prepares required documentation. Represents PPD in the global medical research community and develops
collaborative relationships with investigative sites and client company personnel. Frequent (60% - 80%) travel and long, varied
hours required.
Requirements:
Bachelor?s Degree in life sciences or related field or certification in a related allied health profession from an appropriately accredited
institution (i.e.: RN, MT, PA, RPh, RT)
Minimum of 1 year experience in a clinical environment where experience is gained in clinical trials, medical terminology, medical
research, clinical research, or health care OR a minimum of 2 years experience in a health sciences field with formal training in
medical terminology and anatomy; OR
At least one year of experience as a Clinical Regulatory Specialist with formal training in medical terminology and anatomy;
OR equivalent combination of education, training, and experience that provides the individual a solid background in life sciences,
health care or clinical research.
Effective oral and written English communication skills with ability to communicate effectively with medical personnel
Demonstrated understanding of medical terminology
Strong customer focus
Excellent interpersonal skills
Strong attention to detail
Proven flexibility and adaptability
Basic computer skills and ability to learn appropriate software
Ability to work in a team environment and independently as needed
Ability to successfully complete PPD training program
Preferred:
Degree in Health Sciences
Formal training in physiology
Knowledge in therapeutic and/or clinical specialty to include medical terminology |
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| Project Manager |
The Project Manager is responsible for the overall coordination and management of typically one clinical research project with one
client, in conjunction with the project team. May be responsible for management of multiple protocols.
Education and Experience:
Minimum 1 year supervisory experience.
Minimum 3 years experience in clinical research in clinical monitoring/management combination or program management or clinical
auditing or QA/Regulatory Affairs.
Bachelor's degree in related field or licensed or certified health care training (i.e.: RN, MT, PA, RPh) or equivalent combination of
education, training, and experience that provides the individual with the required knowledge, skills, and abilities.
Knowledge, Skills and Abilities:
Demonstrate leadership skills and ability to manage, motivate, and integrate a team.
Excellent interpersonal skills and problem solving/decision making skills.
Excellent organizational skills.
Demonstrate negotiation skills.
Excellent oral and written English communication skills.
Ability to perform all tasks required of CRA, experience in clinical trials monitoring.
Expert knowledge of FDA/ICH guidelines and GCPs.
Expert knowledge of PPD's Standard Operating Procedures.
Demonstrate knowledge of budgeting/forecasting.
Strong computer skills.
Ability to act as liaison with other Divisions as necessary to complete the study (i.e., Data Management, Biostats, Medical Writing,
Regulatory Compliance, etc.)
Ensures integrity of clinical data
Must be able to multi task and pay close attention to detail |
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