Associate Site Manager

Johnson & Johnson; Hyderabad; On-site; INR 6,00,000 - 8,00,000; Full time

Job summary

A leading healthcare innovator is seeking an Associate, Site Manager in Hyderabad, India. This entry-level site management role requires approximately 2 years of experience in site monitoring and ensures compliance with clinical trial protocols. Responsibilities include serving as the primary contact for trial sites, assisting with recruitment, and performing monitoring activities. Ideal candidates will have a background in clinical trials and compliance oversight.

Qualifications

• Typically requires 2 years of experience in site monitoring.
• Experience in clinical trial protocols and compliance is essential.
• Ability to partner across teams for effective site management.

Responsibilities

• Serve as the primary contact point between the Sponsor and Investigational Site.
• Ensure inspection readiness through compliance with clinical trial protocol.
• Assist with site selection, qualification, and subject recruitment.

Skills

Site monitoring

Good Clinical Practice (GCP)

Clinical trial protocol compliance

Job description

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com

Job Function:

R&D Operations

Job Sub Function:

Clinical Trial Support

Job Category:

Professional

All Job Posting Locations:

Bangalore, Karnataka, India, Hyderabad, Andhra Pradesh, India, Mumbai, India

Job Description:

An Associate, Site Manager is an entry level site management role with typically 2 years of

experience in site monitoring. This role serves as the primary contact point between the Sponsor and the

Investigational Site. An Associate, Site Manager is assigned to trial sites to ensure inspection

readiness through compliance with the clinical trial protocol, company Standard Operating

Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations and guidelines

from study start-up through to site closure. Responsibilities may include assisting with site

selection, site qualification assessment, subject recruitment and retention planning, site

initiation, on-site and remote monitoring and close-out activities. The Associate, Site Manager

will partner with the Local Trial Manager (LTM), Clinical Trial Assistant (CTA) and TDL (Trial

Delivery Leader) to ensure overall site management while performing trial related activities for

assigned protocols. May contribute to process improvement and training. Some supervision

from a more Senior, Site Manager (Senior SM or Lead SM) to help provide guidance to

Associate, Site Manager.