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Syneos Health
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Clinical Research Associate

Clinical Research Associate

Syneos Health

1 - 4 years

3 - 6 Lacs

gurugram

Posted:1 day ago| Platform:

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Skills Required

career development nursing analytical data collection agile clinical research life sciences http recruitment clinical data

Work Mode

Work from Office

Job Type

Full Time

Job Description

Clinical Research Associate

Why Syneos Health

We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
We are committed to our Total Self culture where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
We are continuously building the company we all want to work for and our customers want to work with. WhyBecause when we bring together diversity of thoughts, backgrounds, cultures, and perspectives we re able to create a place where everyone feels like they belong.

Job Responsibilities

Conduct comprehensive on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices and study protocols
Develop and implement tools, procedures, and processes to ensure quality monitoring and adherence to regulatory requirements
Assist in the design, implementation, and delivery of processes, programs, and policies related to clinical monitoring, ensuring alignment with organizational goals
Collaborate with study teams to ensure accurate and timely data collection, entry, and reporting, addressing any discrepancies or issues promptly
Provide guidance and support to lower-level professionals, including training and mentoring, to ensure consistent application of monitoring practices
Manage processes and programs as needed, ensuring efficient and effective operations within the clinical monitoring function
Ensure the integrity and quality of clinical data through regular audits, reviews, and verification of source documents and data entries
Maintain thorough and accurate documentation of monitoring activities, findings, and corrective actions, ensuring compliance with regulatory and organizational standards
Communicate effectively with study sites, investigators, and other stakeholders to address any issues or concerns related to study conduct and monitoring
Stay current with industry trends, regulatory changes, and best practices in clinical research and monitoring, incorporating new knowledge into daily practices

Qualifications:

Bachelors degree in a relevant field such as life sciences, nursing, or a related discipline
Previous experience in clinical research or a related field is preferred
Strong understanding of clinical trial processes and regulations
Excellent organizational and time management skills
Ability to work independently and as part of a team

Certifications:

Certification in clinical research (e.g., CCRP, CCRA) is preferred but not required

Necessary Skills:

Proficiency in using clinical trial management systems and other relevant software
Strong analytical and problem-solving skills
Excellent communication and interpersonal skills
Attention to detail and ability to maintain high standards of quality
Ability to travel as required for on-site monitoring

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