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Job Details

Manager Clinical Operations

Location
Moscow, GORODMOSKVA, Russia, Russia

Posted on
Jun 16, 2020

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Job Information
Bristol Myers Squibb
Manager Clinical Operations
in
Moscow
Russia
Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis.
Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results.
Bristol Myers Squibb Russia
Bristol Myers Squibb has one of the richest biopharmaceutical pipelines in the industry. We discover, develop, and manufacture lifesaving and life altering drugs in in oncology , immune system disease and other therapeutic areas. BMS also has one of the most reliable supply networks and our clinical operations program is among the best and busiest anywhere. We are a company that is forward thinking, a company in which diversity and inclusion are at the forefront of how we view our talent and how we work. Our science is second to none and the transformation work underway will enable us to continue to lead our peer group.
Bristol-Myers Squibb in Russia is seeking to recruit a permanent Manager Clinical Operations
, to ensuring delivery of clinical operations effectiveness in RCO, lead and manage a CTA team, Site Contract Lead and Study Start up Unit.
Key Du
ties and Responsibilities:
Supervises and coordinates the work assignments and performance of Clinical Operations staff inclusive of Clinical Trial Associates (CTAs), Study Start-up Specialists and/or Site Contract Leads to ensure timely execution consistent with R&D and local research goals and priorities
Demonstrates the ability to effectively communicate with and influence individuals at all levels of the organization including situations of conflict resolution, problem solving and crisis management.
Anticipates resource needs and provides workload evaluations and task assignments
Allocates and assign study resources in alignment with R&D and local research goals and priorities.
Supervises clinical trial execution at country level including supervising study metrics and team performance
Approves study fee funds and payments based on grant of authority
May propose and/or validate country study targets
May support Health Authority inspection and pre-inspection activities
May support audit preparation & Corrective Action / Preventative Action preparation for local related issues
Ensure Study Corrective Action / Preventative Action (CAPA) implementation and ensure the necessary resources / tools are available
Develops goals that are consistent with R&D and local research goals and priorities and takes necessary actions to ensure that goals are met
Together with the RCO management tracks and manages performance metrics for Clinical Operations staff
Anticipates and initiates action in response to multiple/changing demands and project priorities placed on Clinical Operations Unit
Point of Contact for FSP staff within the country
Managing the hiring, performance management and succession planning of staff
Performing general and human resource administrative functions
Participation in performance calibration and talent review meetings
Ensuring collaboration and information sharing with local country cross functional stakeholders (Medical, GRS, GPV, Market Access, Commercial, Human Resources)
When managing all RCO staff is delegated to this role in a given country, will represent RCO in local leadership discussions at the affiliate level and may be member of the local affiliate leadership team managed by the General Manager
Ensure effective external partnerships with Study Sites, Investigators, Pharma Trade Associations, Ministry of Health and /or Heath Authorities as needed
Manage partnerships with critical accounts / sites
Qualifications and Experience required:
Bachelors or Masters degree required. Field of study within life sciences or equivalent
Minimum of 5 years Pharmaceutical industry experience in Clinical Research or Medical Affairs
Significant experience in the planning, conduct and management of clinical programs (Phase I-IV)
Demonstrated ability to drive project related activities
Previous supervisory and/or leadership experience (i.e. participation in task force, initiative or cross functional team)
Previous resource allocation experience preferred
Experience mentoring and providing feedback to others
In depth understanding of GCP, ICH Guidelines and other local guidance, regulation and codes of practice related to Clinical Research and Medical Affairs
In depth knowledge and understanding of clinical research processes, regulations and methodology
Understands clinical landscape with practical knowledge of a variety of medical settings and medical records management​
Demonstrated organizational and planning skills and independent decision-making ability
Strong organization and time management skills and ability to effectively manage multiple competing priorities
Outstanding interpersonal, oral and written communication skills to influence, inform or guide others
Good verbal and written communication skills (both in English and local language).
What's important to us
Employees are expected to display the BMS Values, which move us toward our mission to discover, develop and deliver innovative medicines that help patients prevail over serious diseases:
Passion
: Our dedication to learning and excellence helps us to deliver exceptional results.
Innovation
: We pursue disruptive and bold solutions for patients.
Urgency
: We move together with speed and quality because patients are waiting.
Accountability
: We all own BMS ' success and strive to be transparent and deliver on our commitments.
Integrity
: We demonstrate ethics, integrity and quality in everything we do for patients, customers and colleagues.
Inclusion
: We embrace diversity and foster an environment where we can all work together at our full potential.
We have a passion for tackling the toughest diseases, which inspires innovation and speed in our daily work and a sense of accountability to the patients we serve.
Why you should apply
You will help patients in their fight against serious diseases.
You willbe part ofa company that encourages excellence and innovation, respects diversity, develops leaders and values its employees.
You'll get a competitive salary and a great benefits package.
Bristol-Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees the resources to pursue their goals, both at work and in their personal lives.
Company:****
Req Number:
R1525955_EN
Updated:
2020-06-16 00:00:00.000 UTC
Location:
Moscow,Russia
Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.

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