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.

Our global Clinical Operations colleagues within our PPD® clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out, across commercial and government contracts. Together, we help clients define and develop clinical programs, minimize delays, and execute high-quality, cost-efficient clinical studies.

Responsibilities:

Performs remote activities on assigned projects in liaison with the Remote CRA, On-Site CRA and study 
CTM. Provides support with regards to site preparedness, logistical support to the monitoring process,
and assist with assigned tasks for site management and remote monitoring in accordance with SOPs and regulatory guidelines. May be assigned limited site contact activities during study start-up, site 
management, recruitment and close out phases.

Completes study and site management activities as defined in task matrix, and as applicable and directed for study assigned. Completes and documents study-specific training. Orients and trains on any CRG/study-specific systems.Performs remote review of EMR/EHR checklist and supports collection, as applicable assessments. Supports site staff with the vendor related qualification process, where applicable. Provides support by ensuring system access is requested/granted and revoked for relevant site staff during pre-activation and subsequent course of the study. Provides support to follow-up on site staff training, as appplicable. Coordinates and supports logistics for IM attendance, as directed. Supports Essential Document collection, review and updating in systems, as applicable. Follows up and supports on missing study vendor data like ECGs, lab samples, and e-diaries, as directed. Supports ongoing remote review of centralized monitoring tools, as directed. Supports Site payments processes by coordinating with various functional departments within organization and site. Supports system updates and reconciliations, as directed and follows-up on site invoices throughout the study period. Performs reconciliation tasks on assigned trials including but not limited to CRF and query status, deviations, SAEs and safety reports, as applicable. May perform other assigned site management tasks, as directed by RCRA and as per Task Matrix. May perform a specific role profile for FSP opportunities according to Client requests. Maintains & completes administrative tasks such as expense reports and timesheets in a timely manner. 

Education and Experience: 

Bachelor's degree or equivalent and relevant formal academic / vocational qualification 
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years)

Knowledge, Skills and Abilities: 

Basic medical/therapeutic area knowledge and understanding of medical terminology Ability to attain and maintain a working knowledge of ICH GCP, applicable regulations and CRG procedural documents Effective oral and written communication skills Excellent interpersonal and customer service skillsGood organizational and time management skills and strong attention to detail,Proven flexibility and adaptability Ability to work in a team or independently, as required Well-developed critical thinking skills, including but not limited to: critical mindset, in-depth investigation for appropriate root cause analysis and problem solving Proficient computer skills with good knowledge of MS Office ability to learn and use appropriate software. Leverage modern technology when applicable Ability to extract pertinent information from all study documents, electronic study data systems, CTMS and dashboards Excellent English language and grammar skills