CRA - Sr. CRA, FSP, Singapore

Syneos Health, Inc.; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A leading biopharmaceutical solutions organization in Singapore is hiring for a role focused on site management, regulatory compliance, and conducting clinical trials. The ideal candidate will have at least a Bachelor's degree or RN in a related field, excellent communication skills, and be willing to travel up to 75%. This role offers the opportunity to work with innovative projects within a dynamic team aiming to accelerate clinical development and patient success.

Qualifications

• Knowledge of Good Clinical Practice/ICH Guidelines required.
• Ability to manage required travel of up to 75% regularly.
• Willingness to adopt new technologies.

Responsibilities

• Perform site qualification, initiation, monitoring, and close-out visits.
• Manage investigational product inventory and associated risk control.
• Act as primary liaison with study site personnel.

Skills

Communication skills

Presentation skills

Interpersonal skills

Computer skills

Education

Bachelor’s degree or RN in a related field

Job description

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.

Our Clinical Development model brings the customer and the patient to the center of everything we do. We continuously seek ways to simplify and streamline our work to make Syneos Health easier to work with and easier to work for.

Whether you join us in a Functional Service Provider partnership or a Full‑Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile, driven to accelerate delivery, and passionate about changing lives.

Job Responsibilities

• Perform site qualification, site initiation, interim monitoring, site management activities and close‑out visits (on‑site or remotely) to ensure regulatory, ICH‑GCP, and Good Pharmacoepidemiology Practice (GPP) or protocol compliance.
• Verify informed consent procedures, protect confidentiality, assess safety and data integrity risks, and evaluate site performance to provide recommendations and communicate/escalate serious issues.
• Follow the Clinical Monitoring/Site Management Plan (CMP/SMP): assess site processes, conduct source document review, verify CRF data accuracy, resolve queries, and ensure electronic data capture compliance.
• Manage investigational product (IP) inventory, reconciliation, storage, security, dispensing, and associated risk control.
• Review Investigator Site File (ISF) accuracy, reconcile with Trial Master File (TMF), and ensure archiving requirements are met.
• Document activities via letters, reports, logs, and other required project documents per SOPs; support recruitment, retention, and awareness strategies; and enter data into tracking systems.
• Understand project scope, budgets, and timelines; manage site‑level activities and communication to meet objectives and deadlines; adapt quickly to changing priorities.
• Act as primary liaison with study site personnel or collaborate with Central Monitoring Associate; train and ensure compliance of site teams.
• Prepare for and attend investigator meetings, sponsor face‑to‑face meetings, and global clinical monitoring/project staff meetings; attend required clinical training sessions.
• Provide audit‑readiness guidance at the site and project levels and support audit preparation and follow‑up actions.
• Support real‑world late‑phase studies: identify sites, abstract data, collaborate with sponsor affiliates and local country staff, train junior staff, and suggest potential sites based on local knowledge and patient advocacy.

Qualifications

• Bachelor’s degree or RN in a related field or equivalent combination of education, training, and experience.
• Knowledge of Good Clinical Practice/ICH Guidelines and applicable regulatory requirements.
• Good computer skills and willingness to adopt new technologies.
• Excellent communication, presentation, and interpersonal skills.
• Ability to manage required travel of up to 75% on a regular basis.
• US ONLY: Compliance with privacy and facility‑access requirements as part of employment (see company privacy notice).

Get to know Syneos Health

Over the past 5 years, we have worked with 94% of all novel FDA‑approved drugs, 95% of EMA‑authorized products, and over 200 studies across 73,000 sites and 675,000+ trial patients.

Additional Information & Equal Opportunity Statement

Tasks, duties, and responsibilities listed in this job description are not exhaustive. The company, at its sole discretion and with no prior notice, may assign other tasks or responsibilities. Equivalent experience, skills, and/or education will be considered. The company is committed to compliance with the Americans with Disabilities Act, the EU Equality Directive, and provides reasonable accommodations as needed. No contract of employment is created by this description. All applicants are equally considered, and we encourage those who meet the qualifications to apply.