Are you looking to embark on a dynamic career in the pharmaceutical industry? Johnson & Johnson, a global leader in healthcare, is seeking passionate individuals for the position of Associate Site Manager. This entry-level role, based in Mumbai, Maharashtra, offers an excellent opportunity to gain valuable experience in clinical trial support and site management. If you have a background in Pharmacy, Nursing, Life Sciences, or a related scientific field, this could be the perfect role for you!
About the Role
As an Associate Site Manager, you will serve as the primary point of contact between the sponsor and the investigational site. This position revolves around ensuring compliance with clinical trial protocols, company Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations throughout the trial life cycle—from start-up to closure.
In this role, you will collaborate closely with other key roles, including the Local Trial Manager (LTM), Clinical Trial Assistant (CTA), and the Trial Delivery Leader (TDL), to manage trial-related activities efficiently. You will also have the opportunity to contribute to process improvement and training initiatives.
Key Responsibilities
The Principal Responsibilities of the Associate Site Manager include:
- Acting as the primary local contact for assigned sites during specific trials.
- Participating in site feasibility and qualification assessments.
- Attending investigator meetings as required.
- Ensuring site compliance with protocols and conducting on-site and remote monitoring.
- Training site staff and maintaining accurate training records.
- Collaborating with functional areas to enhance site-level recruitment strategies.
- Managing clinical study supplies and ensuring accurate data entry.
You will also be responsible for documenting activities accurately, maintaining regulatory compliance, and fostering effective communication with internal and external stakeholders.
Qualifications and Skills
To be considered for the Associate Site Manager position, candidates must possess the following:
- A BA or BS degree in Pharmacy, Nursing, Life Sciences, or a related field.
- A minimum of 1 year of clinical trial monitoring experience is required (1-2 years preferred).
- Knowledge of GCP, company SOPs, and applicable local regulations.
- Strong IT skills and proficiency in relevant software applications.
- Good written and oral communication skills in English and the local language.
- Willingness to travel and occasionally stay overnight for site visits.
