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Weekend Biotech Project Management Jobs in New York

Job Overview The Senior, Project Management has direct responsibility for the administration and ... Able to work a flexible schedule, including days, evenings, weekends, and holidays, based on ...

... biotechnology, medtech, consumer, and non-profit clients. We deliver insights-driven public ... Reporting to the Director, Project Management, your job will be to own and ensure the timely ...

Legend Biotech is seeking an Operations Manager (2nd Shift) as part of the Technical Operations ... Basic project management skills, responsiveness to issues, and demonstrated passion for creating ...

Legend Biotech is seeking an Operations Manager (2nd Shift) as part of the Technical Operations ... Basic project management skills, responsiveness to issues, and demonstrated passion for creating ...

... in the pharmaceutical and biotech industry devise and implement transformative medical ... Leads project team meetings; * Ensures timely planning and management of client invoicing;

Showing results 21-40

Weekend Biotech Project Management information

What is the difference between Weekend Biotech Project Management vs Weekend Laboratory Technician?

AspectWeekend Biotech Project ManagementWeekend Laboratory Technician
CredentialsBachelor's in Life Sciences or related field; PMP or similar project management certification often preferredAssociate's or Bachelor's in Biology, Chemistry, or related field; relevant lab certifications may be advantageous
Work EnvironmentOffice setting, overseeing biotech projects, coordinating teams, and managing timelinesLaboratory setting, performing experiments, sample analysis, and equipment maintenance
Employer & Industry UsageBiotech firms, research institutions, pharmaceutical companiesResearch labs, biotech companies, academic institutions

Weekend Biotech Project Management focuses on planning, coordinating, and overseeing biotech projects during weekends, requiring project management skills. In contrast, Weekend Laboratory Technicians perform hands-on lab work, conducting experiments and analyzing samples. Both roles are essential in biotech but differ in responsibilities, environment, and required credentials.

What are the key skills and qualifications needed to thrive as a weekend biotech project manager, and why are they important?

To thrive as a Weekend Biotech Project Manager, you need a solid background in life sciences or biotechnology, project management experience, and often a relevant degree or certification such as PMP. Familiarity with project management tools (like MS Project or Asana), regulatory documentation systems, and data analysis platforms is typically required. Exceptional organizational skills, clear communication, and the ability to coordinate cross-functional teams are crucial soft skills. These competencies ensure projects progress smoothly, deadlines are met, and regulatory standards are maintained in a dynamic, results-driven environment.

What is a weekend biotech project manager?

Weekend Biotech Project Managers are professionals who oversee and coordinate biotechnology projects, typically working on weekends or part-time schedules. They are responsible for managing timelines, resources, and teams to ensure projects are completed efficiently and meet regulatory standards. These managers often liaise between research scientists, engineers, and stakeholders to facilitate communication and problem-solving. Their role is especially valuable for organizations with operations that extend beyond traditional work hours or require flexible project management support.

What are the unique challenges of managing biotech projects on weekends, and how can candidates prepare for them?

Weekend Biotech Project Management often involves coordinating work across teams that may have limited availability outside standard business hours. Project managers in this role need to be proactive in communication, ensuring that tasks are clearly defined and any issues are addressed promptly to avoid delays. Flexibility and excellent organizational skills are essential, as you may need to adapt to rapidly changing project needs or unexpected technical hurdles that arise during off-hours. Candidates can prepare by familiarizing themselves with remote collaboration tools and developing strategies for efficient handovers between weekday and weekend teams.
What are the most commonly searched types of Biotech Project Management jobs in New York? The most popular types of Biotech Project Management jobs in New York are:
What are popular job titles related to Weekend Biotech Project Management jobs in New York? For Weekend Biotech Project Management jobs in New York, the most frequently searched job titles are:
What cities in New York are hiring for Weekend Biotech Project Management jobs? Cities in New York with the most Weekend Biotech Project Management job openings:

Associate Director, Project Management - Value & Implementation (VIPM) (Hybrid)

Merck & Co., Inc.

Rahway, NJ • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

This job post has expired today. Applications are no longer accepted.


Merck rating

8.0

Company rating: 8.0 out of 10

Based on 51 frontline employees who took The Breakroom Quiz

43rd of 86 rated pharmaceutical


Job description

Job Description
Global Project and Alliance Management (GPAM) is part of the Research and Development organization at our Company, which is also referred to as our Company's Research Laboratories. GPAM is comprised of Project Managers in Value & Implementation (which is this job), Development, and CMC; Discovery Portfolio Managers; Alliance Managers; Project Management Office (PMO); and Administrative Professionals.
Position Description/Summary:
The GPAM Associate Director, Value & Implementation Project Manager (VIPM), is a core member of Value & Implementation (V&I) Team, partnering with team leaders to develop strategies and execute our Company's drug and vaccine V&I efforts to progress the R&D pipeline and realize its full potential. The Associate Director is expected to provide project management leadership and drive cross-functional teams with sufficient influence and mastery of project management to take on challenging assignments with minimal guidance. Projects could span any therapeutic areas in which our Company is actively engaged. In addition to project work, the Associate Director is expected to contribute to ongoing business process improvement and talent development in GPAM.
This position may be based in either Rahway, NJ; Upper Gwynedd, PA; or Zurich, Switzerland.
Primary Responsibilities:
  • Managing the Value and Implementation process, including projects of significant complexity; driving cross-functional teams and leading by influence to develop comprehensive strategies and ensure successful execution.
  • Act as enterprise leaders by guiding teams through the creation, approval, and execution of integrated project plans appropriate to the project's phase of development and complexity. This includes integrating strategic and tactical input from disciplines (e.g., Medical Affairs, Outcomes Research, Market Access, Biostatistics and Research Decision Sciences, Commercial, and other areas) as applicable to the project.
  • Building and maintaining project plans and critical project information in enterprise project management systems and databases. Using these tools to integrate activities across key team members, proactively identify risks, and ensure clear and effective communication with key team, management, and cross-departmental stakeholders.
  • Leveraging relationships and networks to improve and enhance team dynamics; proactively identifying and removing obstacles to drive business results.
  • Navigating our Company process and organizational norms to enable teams to understand corporate business requirements, thereby enabling decision-making.
  • Leading key team meetings including creating thoughtful agendas, ensuring appropriate participation, contributing project management insights, and following up to ensure the team continues to make progress while holding others accountable.
  • Participating in GPAM departmental initiatives and workstreams aimed at improving the way that we work and the way that we interact with one another as well as other departments. Improving business processes to find new efficiencies and connect people to the information that they need.
  • Providing mentoring, coaching, and oversight to Specialist and Senior Specialist project managers working on common projects. Sharing lessons learned and best practices to impact the GPAM community positively.

Required Education, Experience, and Skills:
  • Bachelor's degree required; concentration in a scientific or applied discipline preferred
  • Minimum of five (5) years of experience in project management or a related role required; in a pharmaceutical/biotech industry preferred

Preferred Experience and Skills:
  • Advanced degree (e.g., MPH, MS, MBA, Ph.D., PharmD) preferred
  • Experience and knowledge of different components of value and implementation strongly preferred; including how the various functional areas contribute to a comprehensive strategy
  • Project management certification (PMP) and/or formal coursework/training in project management strongly preferred

Travel Requirements:
  • 10%

#eligibleforERP
GPAMjobs
#VETJOBS
Required Skills:
Adaptability, Biostatistics, Business Processes, Business Process Improvements, Change Management, Clinical Research, Cross-Functional Leadership, Drug Development, Multiple Therapeutic Areas, Outcomes Research, Process Optimization, Program Implementation, Project Human Resource Management, Project Management Information Systems (PMIS), Project Planning, Publications Management, Regulatory Compliance, Risk Management, Sourcing and Procurement, Strategic Planning, Strategic Thinking
Preferred Skills:
Implementation Management, Implementation Planning, Matrix Leadership
Current Employees apply HERE
Current Contingent Workers apply HERE
US and Puerto Rico Residents Only:
Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.
As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:
EEOC Know Your Rights
EEOC GINA Supplement
We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively.
Learn more about your rights, including under California, Colorado and other US State Acts
The salary range for this role is
$142,400.00 - $224,100.00
This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee's position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.
The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.
We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.
You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.
San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance
Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
Regular
Relocation:
No relocation
VISA Sponsorship:
No
Travel Requirements:
10%
Flexible Work Arrangements:
Hybrid
Shift:
Not Indicated
Valid Driving License:
No
Hazardous Material(s):
n/a
Job Posting End Date:
08/6/2026
*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

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