Study Mgmt Mgr

Company: Innova
Location: Thousand Oaks
Posted on: April 20, 2025

Job Description:

Innova Solutions has a client that is immediately hiring for a Study Mgmt Mgr

In order to make an application, simply read through the following job description and make sure to attach relevant documents.


Position type: Fulltime - Contract
Duration: 36 Months
Location: Thousand Oaks, CA (Remote)


As a Study Mgmt Mgr, you will:

Job Description:
Primary point of contact to lead, manage and coordinate, in partnership with the Contract Research Organization (CRO), the conduct of clinical trials from study design to close out at a global level in accordance with ICH-GCP
Oversee the quality and scientific integrity of clinical operations for studies at a global level

Responsible for:
Global biosimilar development operational execution through oversight of cross functional trial activities in partnership with CRO
Ensuring implementation of trial(s) in partnership with CRO in accordance with applicable SOPs and ICH/GCP guidelines
Execution of clinical studies with high-quality, on time, and within budget
Contribute to the authoring and review of key study documents
Day to day management of study execution including management of study timelines
Managing program-level operational issues and oversight of study team issue escalation
Supports / Leads the Global Clinical Study Team for the allocated program(s)
Communicating global status of clinical study programs to senior management
Contributing to initiatives and process improvement work streams, including process mapping of CROs

Key Activities:
Leads or supports the execution of all studies for a biosimilar program. Includes, but not limited to, PK/PD studies, global pivotal studies, chart reviews, region-specific studies, and device studies as appropriate
Oversee the development of study timelines and budgets for studies within a biosimilar program
Leads or co-leads (with Clinical Data Management) a cross functional team to review clinical study data to ensure high quality deliverables from the CRO
Review and contribute to the creation of study documents, eg, synopsis, protocols, study plans, and Clinical Study Reports (CSR)
Contribute to the execution and oversight of the feasibility process including the development of the site list
Participate in the set-up of study vendors including development of process flow, scopes of work, and budget review
Support global recruitment forecasting, global enrolment, and any recruitment enhancement initiatives
In partnership with the CRO, help organize investigator meetings and study training (eg, CRA training)
Contribute to inspection readiness activities (eg, TMF review, story board generation)
Supports internal audit and regulatory agency inspection readiness activities (eg, TMF review)
Supports / Leads the GCST, ensure operational consistency and standards across all clinical studies within a biosimilar program
Identification and resolution of cross-functional study / program issues within a biosimilar program or escalated from the CRO
Ensure timelines and deliverables are communicated cross functionally and at the CRO
Communicate study status to management
Contribute to development and maintenance of policies, SOPs, and associated documents

Basic Qualifications
Bachelor's degree & 5 years of directly related experience
OR Master's degree & 3 years of directly related experience
OR Doctorate degree & 2 years of directly related experience
Experience with oversight of clinical research organizations (CROs)
Experience in leading cross-functional teams

Preferred Qualifications
7-9 years work experience in life sciences or medically related field, including biopharmaceutical clinical research experience (clinical research experience obtained working on clinical trials at a biotech, pharmaceutical or CRO company)
Experience in oversight of outside vendors (CROs, central labs, etc)

Knowledge
Knowledge of relevant therapeutic or product area
Clinical research experience obtained working on industry-sponsored global clinical trials
Experience working in a global, matrix organization on global clinical development programs
Knowledge to represent and evaluate strategies for clinical development and to critically evaluate outside expert advice
Broad knowledge of Good Clinical Practices (GCP), FDA regulations and guidelines, and international regulatory requirements/guidelines
Solid understanding of Biopharmaceutical/Healthcare Compliance
Experience writing and presenting clearly on scientific and clinical issues


Thank you!
Harish Yadav
Phone: 213-797-4030
harish.yadav@innovasolutions.com

PAY RANGE AND BENEFITS:
Pay Range*: $62.00-$66.00 per hour.
*Pay range offered to a successful candidate will be based on several factors, including the candidate's education, work experience, work location, specific job duties, certifications, etc.

Benefits: Innova Solutions offers benefits( based on eligibility) that include the following: Medical & pharmacy coverage, Dental/vision insurance, 401(k), Health saving account (HSA) and Flexible spending account (FSA), Life Insurance, Pet Insurance, Short term and Long term Disability, Accident & Critical illness coverage, Pre-paid legal & ID theft protection, Sick time, and other types of paid leaves (as required by law), Employee Assistance Program (EAP).

ABOUT INNOVA SOLUTIONS: Founded in 1998 and headquartered in Atlanta, Georgia, Innova Solutions employs approximately 50,000 professionals worldwide and reports an annual revenue approaching $3 Billion. Through our global delivery centers across North America, Asia, and Europe, we deliver strategic technology and business transformation solutions to our clients, enabling them to operate as leaders within their fields.

Recent Recognitions:
Named One of America's Best Employers for New Grads by Forbes (2024
Named One of the Best Companies to Work For by U.S. News & World Report (Private Companies List, 2024-2025)
One of the Largest IT Staffing Firms in the US - Ranked #3 by Staffing Industry Analysts (SIA, 2024)
One of the Largest Staffing Firms in the US - Ranked #13 by Staffing Industry Analysts (SIA, 2024; includes Innova Solutions, Volt, & HireGenics)
Named One of the Top Ten Private Companies in Atlanta by the Atlanta Business Chronicle (2023)
One of the Largest Certified Minority Business Enterprises (MBEs) in the United States (NMSDC, 2024)
AWS Advanced Tier Services Partner with 100+ certifications


Website: https://www.innovasolutions.com/

Innova Solutions is an Equal Opportunity Employer and prohibits any kind of unlawful discrimination and harassment. Innova Solutions is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment on the basis of race, color, religion or belief, national origin, citizenship, social or ethnic origin, sex, age, physical or mental disability, veteran status, marital status, domestic partner status, sexual orientation, or any other status protected by the statutes, rules, and regulations in the locations where it operates. If you are an individual with a disability and need a reasonable accommodation to assist with your job search or application for employment, please contact us at hr@innovasolutions.com or (770) 493-5588. Please indicate the specifics of the assistance needed. Innova Solutions encourages all interested and qualified candidates to apply for employment opportunities. Innova Solutions (HireGenics/Volt) does not discriminate against applicants based on citizenship status, immigration status, or national origin, in accordance with 8 U.S.C. - 1324b.
The company will consider for employment qualified applicants with arrest and conviction records in a manner that complies with the San Francisco Fair Chance Ordinance, the Los Angeles Fair Chance Initiative for Hiring Ordinance, and other applicable laws.

Keywords: Innova, Mission Viejo , Study Mgmt Mgr, Other , Thousand Oaks, California