Step Into Clinical Research with Pharm D Jobs at AstraZeneca Careers
Looking to grow your career through Pharm D Jobs with AstraZeneca Careers? This full-time opportunity is ideal for Pharm D graduates aiming to build expertise in clinical trials and publication management. Through AstraZeneca Careers, professionals in Pharm D Jobs can collaborate with CROs and investigators, manage non-interventional studies, ensure ICH-GCP compliance, and contribute to impactful, patient-focused research initiatives in India.
- Job Title: Project Manager – Trials and Publication
- Location: India (Bengaluru / Chennai)
- Job ID: R-245830
About the Company
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development, and commercialization of prescription medicines for some of the world’s most serious diseases. After 45 years in India, AstraZeneca continues to secure a future where everyone can access affordable, sustainable, innovative healthcare. AstraZeneca Careers offers a Great Place to Work where professionals in Pharm D Jobs are empowered to push the boundaries of science and grow their careers.
Job Description
This Pharm D Jobs opportunity under AstraZeneca Careers involves working in close collaboration with external service providers (CROs) and investigators to ensure quality and quantity commitments are achieved in a timely and efficient manner. The role ensures that studies are conducted in accordance with AZ Procedures, applicable SOP’s & guidelines such as ICH and GCP, and relevant local regulations, while delivering projects as per committed timelines from study start-up to DBL & CSR.
Key Responsibilities
- Works in close collaboration with the external service provider (CRO) and Investigators to ensure quality and quantity commitments are achieved in a timely and efficient manner.
- Responsible for ensuring that the study is conducted in accordance with AZ Procedures/Applicable SOP’s & Guidelines, such as ICH and GCP, as well as relevant local regulations.
- Ensure delivery of the projects according to the commitment & set timelines.
- Initiate, conduct, and deliver non-interventional studies (local, regional, and global) across TAs, External Service Provider Identification, Selection, and Work in close collaboration.
- Initiate ESP contact (CRO, DM, and Laboratory), exchange contracts, and negotiate costs along with the purchase team.
- Prepare the clinical trial budget and get management approval after discussion.
- Assist in designing the study Protocol, CRF, ICF, and other study-related documents.
- Prepare the Monitoring Plan, SDV, and QC plan for the study.
- QC review of study documents, CRO, and ASV, along with the CRO person, to check QC.
- Work with medical colleagues on study protocol and related documents.
- Ensure quality conduct of the trial/study.
- Ensure timely delivery of the project from study start-up to DBL & CSR.
- Publication Management, Adherence to Publication Policy.
Qualifications
Essential:
- Degree or equivalent professional qualification in the related field, Pharm D
- Experience in handling Clinical trials, observational studies, Publication and ESR
Desirable:
-
Post-graduate qualification
