PPD Korea 에서는 아래 포지션에 대해서 지원자를 모집하고 있습니다. 관심 있는 분들의 많은 지원 바랍니다.

지원방법 : 영문이력서(CV) email 발송 Dipika.Dip@ppdi.com / MiJin.Park@ppdi.com

CRA II/Sr.CRA

PPD is aleading global contract research organization. 

At PPD we are passionate, deliberate, and driven by ourpurpose - to improve health.

PPD’s Clinical Monitoring Team is made up ofmonitors with institutional knowledge, in-depth therapeutic experience, and robustoperational tools to help clients define and develop clinical programs,minimize delays, and execute high-quality, cost-efficient clinical studies.

The Clinical Research Associate II/Sr. Clinical Research Associate (CRA) ensuresthe highest quality review of data and effective interaction with study sites.They conduct on-site monitoring visits throughout the study to help our clientdeliver life-changing therapies to patients. The Sr. CRA also performs andcoordinates all aspects of the clinical monitoring and site management processin accordance with ICH Good Clinical Practices, FDA guidelines, localregulations and PPD Standard Operating Procedures. 

Responsibilities:

•  Conducts site visits to assess protocol and regulatory compliance and manages required documentation
• Responsible for ensuring that data will pass international quality assurance audits
• Represents PPD in the global medical research community and develops and maintains collaborative relationships with investigational sites and client company personnel
• May assist project manager or clinical team managers on assigned projects

Grow within the CRA career path to Sr CRA II or PCRA or develop into aline manager role. CRAs often transition to our client dedicated teams and tobecoming CTMs working alongside our Project Management team responsible forclinical deliverables on our studies.

At PPD we hire the best, develop ourselves and each other, and recognize the powerof being one team. It's not just talk - our award winning training programsspeak for themselves.

To learn how PPD can advance your career, apply now!

What To Expect Next

We look forward to receiving your application. Amember of our talent acquisition team will review your qualifications and ifinterested, you will be contacted for an interview.

Qualifications

Education and Experience:

• University degree in a science related field or a certified health care professional or equivalent certification/licensure from an appropriately accredited institution
• Previous experience as a clinical research monitor (comparable to 3+ years) that provides the required knowledge, skills and abilities
• Senior position
• Fluency in English and in the country's native language
• In some cases an equivalent combination of education, professional training, and experience that provides the required knowledge, skills and abilities may be considered
• Preferred with experience in global oncology / Vaccine Study

Knowledge, Skills and Abilities:

• Effective clinical monitoring skills
• Demonstrated understanding of medical/therapeutic area knowledge andmedical terminology
• Excellent understanding and demonstrated application of Good ClinicalPractices and applicable Standard Operating Procedures
• Effective oral and written communication skills, with the ability tocommunicate effectively with medical personnel
• Strong customer focus
• Effective interpersonal skills
• Strong attention to detail
• Effective organizational and time management skills
• Proven flexibility and adaptability
• Ability to work in a team or independently as required
• Good computer skills and knowledge of Microsoft Office with the abilityto learn appropriate software
• Good English language and grammar skills
• Good presentation skills

PPD values the health and wellbeing of our employees. We support andencourage individuals to create a healthy and balanced environment where theycan thrive.  Below is listed the working environment/requirements forthis role:

• Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner
• Able to work upright and stationary for typical working hours
• Able to work in non-traditional work environments
• Able to use and learn standard office equipment and technology withproficiency
• Able to perform successfully under pressure while prioritizing andhandling multiple projects or activities
• May have exposure to potentially hazardous elements typically found inhealthcare or laboratory environments
• This role requires independent travel up to 80%, inclusive of travelingin automobiles, airplanes, and trains.