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1–3 jobs· newest first

COM
Thermo Fisher Scientific · Shanghai, China
Sr. Site Contract Specialist - FSP client dedicated
Thermo Fisher Scientific · Johannesburg, South Africa
Senior
Clinical Trial Coordinator
Thermo Fisher Scientific · Remote, Singapore
Remote

+10K new in the last hour

COM

Thermo Fisher Scientific · Posted Jul 7, 2026

Shanghai, China
5+ years

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Manages, selects, trains, resources, coaches and performance management of clinical operations staff.

Responsibilities

Manages staff, providing coaching, mentorship and work direction
Conducts regular performance appraisals and career discussions with staff
Facilitates employee career development
Interviews, recruits and selects staff
Manages and conducts induction/orientation programs for all new employees

Requirements

Bachelor's degree or equivalent

Skills

mentoring leadership supervisory clinical trials monitoring SOPs WPDs ICH/GCP FDA guidelines data entry travel Activate CTMS Preclarus Clarity

Benefits

competitive remuneration
annual incentive plan bonus
healthcare
range of employee benefits

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Sr. Site Contract Specialist - FSP client dedicated

Thermo Fisher Scientific · Posted Jun 28, 2026

Johannesburg, Gauteng, South Africa
Senior
5+ years

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Senior Site Contract Specialist managing contract preparation, negotiation and finalization with study sites, ensuring compliance and risk analysis.

Responsibilities

Draft, review, negotiate and finalize agreements with study sites
Negotiate within approved parameters
Ensure compliance to established negotiation parameters
Identify and assess legal, financial and operational risks
Provide recommendations and alternative resolutions

Requirements

Bachelor's degree or equivalent

Skills

contract law negotiation analytical thinking risk analysis pharmaceutical product development process CRO involvement attention to detail time management

Clinical Trial Coordinator

Thermo Fisher Scientific · Posted Oct 27, 2026

Remote, Singapore
Remote
0–1 years

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Provide administrative and technical support for clinical trial projects, ensuring audit readiness, site activation, and regulatory compliance.

Responsibilities

Coordinate and oversee trial activities as per task matrix
Perform internal, country and investigator file reviews
Ensure tasks are completed on time and within budget
Provide system support for Activate & eTMF
Process documents for client eTMF

Requirements

High / Secondary school diploma or equivalent
Bachelor's degree preferred

Skills

Teamwork Organizational skills Attention to detail Project data analysis Customer focus Flexibility Knowledge of Country Regulations ICH Good Clinical Practices

organizational skills

automated systems

computerized applications

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English language

Local language skills

Computer skills

Clinical trial database systems

Clinical training program

Interpersonal skills

Oral and written communication

Judgment and decision-making

Risk management

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