Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.  

We are currently hiring Clin Ops Delivery Specialist (RSM-C I).

Major responsibilities:

Works highly independent and performs critical assessments in collaboration with study teams or other departments to determine best approaches to manipulate subject data. The RSM-C is capable of leading active and challenging interdepartmental discussions to explore best strategies and practices after understanding trial specific needs and diverse data bases that can be used as source of information.

Reviews subject data from multiple sources with a data analytic mindset, capable of identifying trends, risks, gaps and areas for optimization as the subject data and the trial develops. Prepares and analyzes clinical trial patient datasets. Adapts to constant changes as trial develops. Capable of providing concise and clear updates to study teams and other key stakeholders after processing and reviewing subject data.

Continually makes efforts to increase knowledge base and professional skills in areas such as programming, technology and techniques, clinical trials, and the pharmaceutical industry by working closely with mentors, attending presentation / teaching events, and contributing to other general department documents and policies by assisting mentors with implementing best practice documents and articles.

The RSM-Central generates a thorough understanding of protocol schedule of events (visits, activities and procedures), Contracts, budgets and/or payment terms. 

Escalates performance issues to clinical, site payments and IT managers and may assist with resolution (Follows Escalation Pathway as applicable). Lead internal team meetings and provide updates on subject data statuses. Manage escalations (project team, site and sponsor) regarding tracking system setup/maintenance issues. 

Qualifications and Skills (some of the below are desired):

Bachelor's degree in life science-related fields, Engineering, Biostatistics and/or Programing or related fields/degreesIf possible (but not required), prior clinical research experience or related fields of minimum 6 months to 1 year or related experience involving knowledge of clinical trials.If possible (but not required), prior experience of minimum 6 months to 1year on process development or process improvement.If possible (but not required), prior experience of minimum 6 months to 1year on data assessments, analytics or critical assessments.Highly independent and capable of leading multidisciplinary discussions as needed.Comfortable with decision making and proper documentation practices.Capable of working under continuous pressure and continuous changing challenges adapting to new priorities and needs as they arise.If possible (but not required), experience with data bases with scientific background.

Skills and abilities:

Understanding of data base structure and complex data systemsProven understanding and use of Microsoft Excel Capable of effectively capturing and reviewing dataCapable of providing quality control support Good attention to detailGood problem-solving skillsExcellent written and verbal communications skills to effectively interface with teams, including proficiency in the English languageCapable of effectively organizing and managing multiple assignments with challenging timelinesCapable of adapting and adjusting to changing prioritiesPositive attitude and the ability to work well with othersDemonstrate initiative and self-motivation

What we offer:

At PPD clinical research services we hire the best, develop ourselves and each other, and recognize the power of being one team. We understand that you will want to grow both professionally and personally throughout your career, and therefore at PPD clinical research services you will benefit from an award-winning learning and development programme, ensuring you reach your potential.

As well as being rewarded a competitive salary, we have an extensive benefits package based around the health and well-being of our employees. We have a flexible working culture, where PPD clinical research services truly value a work-life balance. We’ve grown sustainably year on year but continue to offer a collaborative environment, with teams of colleagues eager to share expertise and have fun together. We are a global organization but with a local feel.

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status