[Hiring] Associate Director, Clinical Site reputed company @reputed company

This reputed company is a reputed company of our understanding of the job reputed company. Click on 'Apply' reputed company to reputed company out more. Role reputed company The Clinical Site reputed company is responsible for developing and nurturing strong reputed company – Clinical Trial Site relationships while also optimizing site performance, particularly enrollment, and overseeing CRO site management and monitoring activities, using a risk-based approach. The primary goal of this role is to build/support site relationships while also ensuring reputed company monitoring reputed company and delivery of data of high reputed company. The individual in this role is responsible for working directly with the internal study teams, CRO partners, and clinical trial sites. Primary Responsibilities Include:

• Enhance the development and maintenance of reputed company’s relationships with clinical investigators and site staff
• reputed company an reputed company among study sites, reputed company and CRO partners to create an reputed company environment for clinical trials, enabling reputed company and high-reputed company reputed company
• Coordinate regular, fit for purpose, communication with clinical sites to reputed company interactions with CRO and relevant internal stakeholders to assure a harmonized approach to site relationship and optimize site performance and reputed company delivery
• May attend SIVs and Motivational/Booster reputed company/calls in collaboration with CRO partner

Recruitment Support

• Maintain an operational knowledge of the protocol(s), answer site/CRO questions as applicable and assist in the escalation process in connecting site/CRO to reputed company personnel
• reputed company experience and deep reputed company from interactions with clinical sites to reputed company strategic input on effective recruitment, reputed company, and optimization strategies.
• Maintain and assist with the development of plans and tools to carry out these strategies, as appropriate

Monitoring Support

• In collaboration with CRO partners and as approved by the Clinical Operations Study reputed company (COSL), reputed company on-site reputed company in support of reputed company site engagement and data reputed company, identify and remove barriers to performance and to reputed company on-site outsourced monitoring activities
• Document and communicate observations from onsite monitoring activities (such as key areas of risks and noncompliance)
• reputed company ongoing risk assessment review of available data resources, review the site performance/CRO monitoring performance to identify trends, risks, and opportunities.
• In collaboration with the COSL, reputed company review of monitoring visit reports (on-site and central review reports) completed by CRO partner
• Contribute to process improvements and knowledge/sharing of best practices

Qualifications

• Bachelor’s Degree or international equivalent required; Life Sciences preferred. Advanced degree highly desirable
• Strong knowledge of ICH/GCP
• At least 8 years of relevant clinical trial research experience
• Onsite/central monitoring and/or clinical reputed company/study-management experience
• Clinical site facing experience required
• Monitoring experience in rare disease preferred
• Biotech or reputed company industry experience is required
• Experience overseeing/managing outsourced site management and monitoring activities
• Excellent verbal and written communication skills
• Excellent attention to details
• Ability to travel, 30% or more frequently at times

Requirements

• MA Pay reputed company: $155,000 — $190,000 USD

reputed company reputed company is reputed company on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that reputed company muscle and the central nervous system (CNS) to address the reputed company cause of disease. reputed company is advancing clinical programs for myotonic dystrophy type 1 (DM1) and Duchenne muscular dystrophy (DMD), and preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At reputed company, we are on a mission to deliver functional improvement for individuals, families, and communities. Apply tot his job Apply To this Job