Clinical Coordinator Pfizer Inc. Surat, Gujarat
Pfizer is the world’s premier biopharmaceutical company taking new approaches to better health. We discover, develop, manufacture and deliver quality, safe and effective prescription medicines to treat and help prevent disease for people. We also partner with healthcare providers, governments and local communities around the world to expand access to our medicines and to provide better quality health care and health system support. At Pfizer, colleagues in more than 90 countries work every day to help people stay happier and healthier longer and to reduce the human and economic burden of disease worldwide. Our Pfizer Clinical Research Unit (PCRU) in Brussels is a state-of-the-art research facility with sixty inpatient beds dedicated to early clinical trials (Phase 1 & 2a studies). The Clinical Coordinator assures and is responsible for the protocol adherence and data quality of assigned protocols in the PCRU Brussels Clinical Services operations in accordance with scientific, medical and ethical principles and with regulatory requirement guidelines JOB RESPONSIBILITIES Demonstrates professional study related communication and responsible for data integrity, oversees quality and completeness and documentation on an ongoing basis (electronic and written) Ensures that appopriate staff is trained for study execution Supports the planning and scheduling team to identify sufficient resources Ensures close follow up on study queries QUALIFICATIONS / SKILLS Minimum of a Bachelor Degree ( Life Science/Biomedical or Health Care related training). Minimum of 1 year of relevant work experience in in pharmaceutical or medical research (Prior experience in Phase 1 or exploratory research is advantageous). Experience in the delivery of scientific educational presentations. Recognized internally and externally as technical/functional expert in Phase I Clinical Operations and relevant disciplines. Excellent working knowledge of computers and and laboratory data handling acquisition systems and associated issues/risks Excellent knowledge of medical conditions, nursing and research techniques, and application of clinical research Ability to review and understand emerging safety and efficacy profile of a drug candidate and recognize potential serious adverse effects. Ability to align clinical skill sets with protocol requirements to assure appropriate staffing for studies Demonstrated understanding of the complexities and recent developments in exploratory research. Understanding of clinical pharmacology issues Exposure to exploratory development strategies and full development activities Good written and verbal skills in English, French and Dutch are essential Finance awareness Ability to communicate in easily understandable language for complicated research principles. Must be able to instruct and assist less skilled or inexperienced personnel in the performance of study activities. Team Work Participation in multifunctional, interdepartmental management teams. Able to lead multi-disciplinary groups; ability to manage and motivate Comfortable with implementing change, Business oriented Challenges existing paradigms in clinical research and encourages novel study designs and research approaches; works to improve study conduct and data capture Identifies and builds effective relationships with customers and other stakeholders ORGANIZATIONAL RELATIONSHIPS Reports to PCRU Clinical Coordination Manager Matrixed relationship with relevant PCRU study team members WHAT WE CAN OFFER In addition to competitive salaries and customized benefits packages, we offer a supportive and diverse culture and unparalleled career development opportunities. For all our projects regarding diversity and inclusion on the work floor, Pfizer is closely collaborating with Actiris. Candidates will be contacted by email or telephone within a maximum of 4 weeks from the end of the advertisement. Thanks for your patience and understanding