Site Care Partner - FSP (Senior/Lead CRA)

My research opens up

new medical possibilities.

And I do it

Search Jobs

Search Jobs

Keyword

Matching job links will appear below as you type.

Location: When autocomplete results are available use up and down arrows to review and enter to select. Touch device users, explore by touch or with swipe gestures.

Radius: Enter distance 5 15 25 35 50

Unit MILES KM

View Remote Jobs View All Jobs

View remote jobs View all jobs

Site Care Partner - FSP (Senior/Lead CRA)

Primary Location: South Korea, Remote Job ID R0000045923 Category Clinical Trials Date Posted 09/15/2026

Apply Now

• Success profile
• About this role
• Potential career path
• Employee insights
• Our team
• Why Clinical Research Associates work at Parexel
• Learn about our culture
  
  

Overview

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part to get treatments to patients sooner. Our CRAs' priority is the safety and well-being of the patients. As you travel to investigator sites and perform your monitoring duties, we encourage you to be inquisitive, take accountability, build relationships, and act with integrity.

Join a team with a wide variety of experiences and knowledge, and work on global projects within a broad scope of therapeutic areas. We’re looking for people who want to grow personally and professionally and support their colleagues globally and cross-functionally.

Success Profile

Do you have these soft skills and interpersonal traits to succeed at Parexel?

• Communicator
• Detail-oriented
• Flexible
• Organized
• Problem-solver
• Self-starter
  
  

Back to nav

About This Role

At least 8+ years of CRA experience is required.

Must Have Oncology Study Experience.

Experience in other therapeutic area would be a plus.

Key Accountabilities

Site start-up and activation

• Deploys client site strategies by qualifying and activating assigned sites
• Supports processes to optimize country & site selection activities including review and assessment of the draft potential site list and provide site qualification output for site selection
• Collaborates with key stakeholders providing country/regional level input to country outreach surveys including protocol feasibility, country Standard of Care (SOC) and medical practices (as applicable) under supervision
• Maintains a knowledge of assigned protocols
• Conducts study start-up activities at the site level including but not limited to Site Qualification, coordination of site activation checklist items, Informed Consent Form (ICF) finalization, Site Initiation Visit (SIV) as applicable, including management of issues that may compromise time to site activation
• Ensures all the site initiation activity including training per site activation checklist, collect and / complete necessary documentation/ systems needed for site activation
• Supports country specific ICF review and deployment up to Site Activation
• Ensures follow up activities’ completion post Site qualification visit and SIV to ensure site readiness for First Subject First Visit (FSFV)
• Partners with Clinical Research Associate (CRA) to ensure site monitoring readiness in anticipation of FSFV
• Responsible for relationship building and operational quality of the site
• Responsible for establishing and maintaining relationships with Site Organizations and Strategic Partners
• Provides study support on escalated site issues related to study delivery by coordinating communications and resolution efforts. (e.g., vendor, site contracts and payment issues etc.)
• Ensures the strategy and approach for Investigational Product (IP) and ancillary supplies for sites and country requirement throughout the lifecycle of the study
• Accountable for effective site recruitment planning and delivery, consistent with global and/or country plan and local targets; Jointly responsible with CRA for enrollment delivery during study conduct
• Partners with local Regulatory authorities and Study Start up teams to ensure timely completion on country / local registry up to Site Activation
  
  

Intelligence gathering

• Provides input into site recommendations via intimate understanding of country/region, sites, processes and practices, and associated site performance metrics
• Provides support to study management to define local requirements for the importation/exportation processes of the investigational medical product and ancillary supplies
  
  

Study conduct and close-out

• Reviews Site Reports and related issues
• Assures quality and consistency in the delivery of monitoring
• Supports the CRA to develop positive Investigator relationships throughout the life of the study and escalate any training or compliance concerns with Study Management
  
  

Compliance with Parexel standards

• Complies with required training curriculum
• Completes timesheets accurately as required
• Submits expense reports as required
• Updates CV as required
• Maintains a working knowledge of and complies with Parexel processes, ICH-GCPs, and other applicable requirements
  
  

Skills

• Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements
• Must demonstrate good computer skills and be able to embrace new technologies
• Good communication, presentation, and interpersonal skills
• Ability to manage required travel
• Demonstrated networking and relationship building skills
• Demonstrated ability to manage cross functional relationships
• Ability to communicate effectively and appropriately with internal & external stakeholders
• Ability to adapt to changing technologies and processes
• Knowledge of country requirements for GCP that may be different to those of client procedures
• Effectively overcoming barriers encountered during the implementation of new processes and systems
• Identifies and builds effective relationships with investigator site staff and other stakeholders
• Effective verbal and written communication skills in relating to colleagues and associates both inside and outside of the organization
• Able to manage issues that are escalated by site staff in a way that meets the needs of both the client and the site staff
  
  

Knowledge And Experience

• Demonstrated experience (8+ years) in site management with prior experience as a CRA
• Demonstrated experience in start-up activities through site activation
• Demonstrated experience in conduct and close out activities
• Demonstrated knowledge of quality and regulatory requirements in applicable countries
  
  

Education

• Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience (estimate at least 5 years’ experience)
• Proficiency in local language preferred. English is required
  
  

Back to nav

Share this job

• LinkedIn
• Facebook
• X
• Email
  
  

Potential Career Path

Parexel offers various career paths and internal development programs for CRAs to advance to the next level. This could include enhancing your technical position, moving into management, or shifting to other areas of the business.

• APEX CRA
• CRA I
• CRA II
• Senior CRA
• Project Management
  
  

Subject Matter Expert

People Management

Back to nav

Employee Insights

Nick on a day in the life of a CRA

Nick Burger | Senior Clinical Research Associate

Watch Video

Liliana on CRA tasks and our recognition program

Liliana Belmares Flores | CRA Line Manager

Watch Video

Marlayna on why Parexel is a great place for CRAs

Marlayna Fitts | CRA Line Manager

Watch Video

Back to nav

TEAM IMPRESSIONS

Back to nav

Why Clinical Research Associates work at Parexel

Patient-focused in everything we do

We push the boundaries of what is possible to create clinical trials that are inclusive, innovative, and patient-focused

Supportive and inclusive environment

We foster collaboration, teamwork, respect, and inclusivity, to work together to achieve common goals.

Career growth and development

We develop your skills through training, mentorship, and career advancement programs.

Flexible work arrangements

We focus on outputs and results, not where and when you work.

Diverse therapeutic areas and project exposure

We continuously learn from a broad exposure from early to late phase clinical trials and our cros-functional global teams.

Advanced Technology

We recognize the importance of first-time quality to bring treatments to patients faster.

Back to nav

Learn About Our Culture

Back to nav

Back to nav

• Meet Stacy Hurt, Chief Patient Officer at Parexel
  
  

Insights on Parexel's patient-centric approach, innovative strategies, and authentic culture in clinical research. Learn how Stacy's unique experiences shape the future of clinical trials.

Learn More

• Meet Hina, an Executive Director championing excellence and empathy
  
  

Parexel's Hina Saleem, Executive Director, Clinical Operations, shares how empathy and excellence drive her approach to clinical trial optimization and authentic leadership.

Learn More

• Meet Adriane, a Senior Clinical Operations Leader sharing insights and tips
  
  

Discover Adriane's role as a Clinical Operations Leader. She shares insights into her daily responsibilities, the skills crucial for success, and the rewarding challenges she faces. Learn how Parexel supported her career development and gain inspiration from her advice on professional growth.

Learn More

• Working as a Nurse in Clinical Research at Parexel
  
  

Antje and Katharina share insights into working as a Nurse in Clinical Research, where innovative medications are developed through early-phase and first-in-human studies.

Learn More

• Video on Working With Heart® - Christina's Clinical Operations Manager Perspective
  
  

View how Christina reflects on her work experience, her impact on patients and her management style of respect and growth. Christina is leading a team of Clinical Operations Leaders who manage groundbreaking trials in the biotech space.

Learn More

• Meet Andrea: Senior Initiation Clinical Research Associate
  
  

Andrea's story shows how teamwork, attention to detail and patient focus drive success at Parexel while finding fulfillment in helping innovative treatments reach patients faster.

Learn More

• Meet Yena, a Site Contracts Associate
  
  

Yena shares her inspiring journey from nursing to clinical research, highlighting how Parexel supports career growth and work-life balance. Learn about the critical role of Site Contracts Associates and what it means to work 'With Heart'.

Learn More

• Optimizing the clinical research workforce: An industry analysis by Parexel
  
  

This comprehensive report benchmarks the trends and innovations having the greatest impact on drug development and identifies the skills required for today’s workforce.

Learn More

• Meet Julie, a Senior Clinical Assistant, proud of her contribution
  
  

Julie welcomes volunteers at the Early Phase Clinic reception in Berlin, manages payments, and caters to the volunteers in the kitchen.

Learn More

• Meet Alexis, a Clinical Research Associate II championing patient care
  
  

Alexis progressed from Administrative Assistant to CRA via Parexel's APEX program. She passionately works for the patients, sites and coworkers to make a difference. Off-duty, she enjoys time with her poodle, Millie, and baking shows.

Learn More

• Meet Margaret: Clinical Research Nurse
  
  

Find out why Margaret enjoys working as a Nurse in Clinical Research and working at Parexel, also how Parexel supports her in a way she hasn't experienced anywhere else.

Learn More

• Meet Theodora, a Site Contract Leader
  
  

Theodora Chung offers us an insight into her role, which is to oversee the clinical trial budgets and contracts. From planning and drafting to negotiations up to execution.

Learn More

• Meet David, a champion for disability inclusion
  
  

His leadership fosters workplace and clinical research inclusivity. Explore David's inspiring journey from combat medic to Parexel VP and Disability Inclusion Business Resource Group co-lead.

Learn More

• Meet Laurias: Manager, Clinical Operations
  
  

Laurias shares how Parexel has supported his career development from CRA to Clin Ops Manager and flexibility within the workplace.

Learn More

• Meet iCRA Twins Marina Palumbo and Anna Korelis
  
  

Double the passion and double the commitment to working With Heart™. Read on to learn more about these colleagues whose family and work lives are uniquely intertwined at Parexel!

Learn More

• Clinical Operations Opportunities
  
  

Are you passionate about making a difference in the fight against cancer and beyond? At Parexel's Global Clinical Operations, we are dedicated to putting patients at the heart of every clinical trial. With a global footprint and 5000 Clinical Operations team members worldwide, we are impacting clinical research.

Learn More

• Benefits & Support
  
  

At Parexel, we prioritize putting people first, allowing you to achieve your best work. Explore the Flexible Work Program, our "Bravo" Recognition Program, and how we build our well-being in our supportive culture.

Learn More

• Inclusion at Parexel
  
  

Learn how Parexel celebrates the differences our workforce and patients bring and ensures an inclusive environment.

Learn More

• Emerging Talent Opportunities
  
  

Begin your career journey at Parexel with our emerging talent programs or our internships, placements and entry-level clinical roles. Advance science by keeping the patients in mind.

Learn More